Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

INTRA-MEDULLARY ALIGNMENT, GUIDE BUSHING, LPI BETA ARC, 6° 10mm

Registry build 21.09.26
21manufacturers in China registered for this device type
584catalogue numbers in this listing
32510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Beijing (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JWH
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Changzhou Wastonortho Medical Appliance Co., Ltd. Changzhou Jiangsu Contract manufacturer 5

Showing 12 of 21. All 21 manufacturers in China registered for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Record

Regulatory record for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Listed by Exactech, Inc., United States
FDA product code JWH
Device type Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3560
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K033883
Record published 2022-08-18
Record revised 2026-02-09 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, serial number
Sizes Angle 2 to 7 °; lumen/inner diameter 3.2 to 53 mm; outer diameter 3.17 to 29 mm; width 2 to 65 mm; outer diameter 0.188 to 250 in; length 11 to 30 mm
Distribution end date 2024-06-13

Catalogue Numbers

Catalogue numbers for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Catalogue number Size Status
213-50-51 SIZE 1 In distribution
201-85-00 In distribution
209-04-73 SIZE 3 In distribution
105-02-45 4.5mm In distribution
213-56-10 SIZE 0 In distribution
213-52-19 In distribution
201-90-01 In distribution
209-04-41 SIZE 3 In distribution
02-019-66-0210 Width 29 mm In distribution
02-019-66-0222 Width 32 mm In distribution
213-51-01 SIZE 1 In distribution
213-41-06 In distribution
213-53-25 SIZE 5 In distribution
02-019-30-0100 Outer Diameter 10 mm In distribution
207-48-00 In distribution
213-51-53 SIZE 3.5 In distribution
213-64-41 Width 41 mm In distribution
213-52-15 In distribution
02-019-50-0299 In distribution
SPI-037148 In distribution
213-41-04 In distribution
201-51-51 SIZE 1.5 In distribution
02-019-66-0221 Width 29 mm In distribution
209-04-12 SIZE 1 In distribution
213-65-05 In distribution
02-019-30-0201 In distribution
201-13-04 SIZE 4 In distribution
213-58-15 SIZE 5 In distribution
02-019-66-0004 In distribution
02-019-30-0301 In distribution
207-10-02 In distribution
213-63-23 Width 23 mm In distribution
02-019-70-0007 In distribution
201-13-02 SIZE 2 In distribution
213-65-01 SIZE 0-1-2 In distribution
213-56-00 0 Degree In distribution
213-53-24 SIZE 4 In distribution
209-04-31 SIZE 3 In distribution
213-46-05 Angle 5 ° In distribution
02-019-30-0004 Width 4 mm In distribution
02-019-66-0260 Width 65 mm In distribution
105-02-32 3.2mm In distribution
213-73-15 In distribution
201-13-13 Angle 3 ° In distribution
207-80-00 In distribution
201-51-53 SIZE 3.5 In distribution
213-50-53 SIZE 3 In distribution
213-50-12 SIZE 2 In distribution
213-60-03 Lumen/Inner Diameter 29 mm In distribution
213-51-05 SIZE 5 In distribution
213-56-15 SIZE 5 In distribution
207-80-10 In distribution
209-71-16 Lumen/Inner Diameter 16 mm In distribution
213-53-21 SIZE 1 In distribution
209-56-20 Outer Diameter 20 mm In distribution
205-56-02 Outer Diameter 13 mm In distribution
213-74-04 SIZE 1-1.5-2 In distribution
201-59-06 Lumen/Inner Diameter 26 mm In distribution
213-60-08 In distribution
213-48-00 0 Degree In distribution
213-58-51 SIZE 1.5 In distribution
213-53-13 SIZE 3 In distribution
205-56-07 Outer Diameter 23 mm In distribution
207-60-00 In distribution
209-04-22 SIZE 3 In distribution
207-10-08 In distribution
213-51-10 SIZE 0 In distribution
213-51-11 SIZE 1 In distribution
207-10-07 In distribution
213-58-53 SIZE 3.5 In distribution
213-53-06 SIZE 6 In distribution
213-03-17 Angle 7 ° In distribution
205-56-04 Outer Diameter 17 mm In distribution
02-019-66-0120 MEDIUM In distribution
213-53-05 SIZE 5 In distribution
207-60-02 In distribution
213-58-16 SIZE 6 In distribution
02-019-66-0240 Width 48 mm In distribution
02-019-30-0202 In distribution
209-45-07 Angle 7 ° In distribution
213-41-02 In distribution
213-58-11 SIZE 1 In distribution
02-019-50-0110 SIZE 1 In distribution
201-51-52 SIZE 2.5 In distribution
201-59-29 Outer Diameter 29 mm In distribution
213-52-14 In distribution
213-56-03 Angle 5 ° In distribution
211-53-01 SIZE 1 In distribution
201-71-12 12mm In distribution
205-56-05 Outer Diameter 19 mm In distribution
213-74-11 SIZE 4.5-5-6 In distribution
209-56-22 Outer Diameter 22 mm In distribution
213-46-06 Angle 5 ° In distribution
02-019-66-0002 In distribution
213-56-13 SIZE 3 In distribution
02-019-30-0203 In distribution
207-80-01 In distribution
201-56-00 0 Degree In distribution
213-56-51 SIZE 1.5 In distribution
209-71-14 Lumen/Inner Diameter 14 mm In distribution
207-10-01 In distribution
02-019-66-0224 Width 48 mm In distribution
205-75-02 SIZE 2 In distribution
209-56-16 Outer Diameter 16 mm In distribution
02-019-66-0005 In distribution
209-04-72 SIZE 2 In distribution
213-50-14 SIZE 4 In distribution
02-029-11-1000 In distribution
213-50-16 SIZE 6 In distribution
213-65-00 In distribution
201-51-77 SIZE 2.5 In distribution
209-53-01 SIZE 1 In distribution
02-019-30-0113 Outer Diameter 12 mm In distribution
213-50-35 SIZE 5 In distribution
213-53-12 SIZE 2 In distribution
231-04-02 In distribution
213-64-53 Width 53 mm In distribution
213-58-52 SIZE 2.5 In distribution
211-53-02 SIZE 2 In distribution
213-48-01 RIGHT In distribution
213-58-14 SIZE 4 In distribution
201-59-26 Outer Diameter 26 mm In distribution
201-59-23 Outer Diameter 23 mm In distribution
213-74-00 In distribution
209-43-00 In distribution
181-00-06 Lumen/Inner Diameter 3.2 mm In distribution
207-60-01 Outer Diameter 9 mm In distribution
213-74-10 SIZE 2.5-3-3.5-4 In distribution
02-019-66-0220 Width 32 mm In distribution
213-03-14 Angle 4 ° In distribution
201-41-00 In distribution
213-56-06 +2 In distribution
213-73-17 In distribution
207-47-00 In distribution
213-65-04 In distribution
213-53-15 SIZE 5 In distribution
213-46-07 Angle 7 ° In distribution
201-59-01 In distribution
209-56-18 Outer Diameter 18 mm In distribution
213-74-12 SIZE 0 In distribution
02-019-50-0003 In distribution
213-58-10 SIZE 0 In distribution
209-04-74 SIZE 4 In distribution
209-51-01 SIZE 1 In distribution
201-51-22 1/8″ Pegs In distribution
213-73-07 In distribution
213-50-03 SIZE 3 In distribution
209-53-05 SIZE 5 In distribution
02-029-12-1000 In distribution
209-89-00 In distribution
02-019-30-0302 In distribution
209-46-05 Angle 5 ° In distribution
02-019-66-0007 In distribution
201-59-09 Lumen/Inner Diameter 29 mm In distribution
209-04-71 SIZE 1 In distribution
209-30-00 In distribution
209-53-04 SIZE 4 In distribution
209-56-14 Outer Diameter 14 mm In distribution
213-53-22 SIZE 2 In distribution
213-51-14 SIZE 4 In distribution
213-50-32 SIZE 2 In distribution
02-019-70-0004 In distribution
213-48-02 LEFT In distribution
207-80-03 In distribution
213-62-35 Lumen/Inner Diameter 35 mm In distribution
02-019-66-0250 Width 57 mm In distribution
213-46-02 Angle 2 ° In distribution
209-57-00 Width 3.5 mm In distribution
02-019-66-0110 SMALL In distribution
213-73-18 In distribution
02-029-19-1310 In distribution
213-58-12 SIZE 2 In distribution
213-51-06 SIZE 6 In distribution
209-45-05 Angle 5 ° In distribution
213-03-07 Angle 7 ° In distribution
201-83-78 SIZE 3.5 In distribution
213-50-06 SIZE 6 In distribution
02-019-50-0004 In distribution
209-51-02 SIZE 2 In distribution
209-89-05 In distribution
02-019-66-0225 Width 57 mm In distribution
213-50-02 SIZE 2 In distribution
213-64-47 Width 47 mm In distribution
213-63-00 In distribution
02-019-30-0000 0 mm In distribution
213-03-16 Lumen/Inner Diameter 10 mm In distribution
213-51-15 SIZE 5 In distribution
213-41-03 In distribution
207-80-02 In distribution
213-03-12 Lumen/Inner Diameter 10 mm In distribution
213-53-04 SIZE 4 In distribution
213-53-14 SIZE 4 In distribution
213-53-03 SIZE 3 In distribution
207-10-00 In distribution
209-71-18 Lumen/Inner Diameter 18 mm In distribution
213-74-09 SIZE 1-1.5-2 In distribution
02-019-66-0223 Width 39 mm In distribution
211-53-03 SIZE 3 In distribution
213-56-17 In distribution
105-02-01 In distribution
231-04-03 In distribution
213-60-05 Lumen/Inner Diameter 35 mm In distribution
201-13-06 SIZE 6 In distribution
209-04-21 SIZE 2 In distribution
207-10-09 In distribution
209-53-02 SIZE 2 In distribution
201-58-02 In distribution
02-019-66-0000 In distribution
201-83-77 SIZE 2.5 In distribution
201-61-13 Outer Diameter 0.188 in In distribution
207-60-07 In distribution
02-019-30-0115 Outer Diameter 15 mm In distribution
02-019-66-0006 SMALL In distribution
211-53-05 In distribution
213-83-00 In distribution
213-65-03 SIZE 5-6 In distribution
213-73-00 In distribution
02-019-10-0220 SIZE 2 In distribution
213-83-02 In distribution
213-77-00 In distribution
209-51-04 SIZE 4 In distribution
02-019-70-0005 In distribution
02-019-10-0250 SIZE 5 In distribution
213-83-12 In distribution
213-64-35 Width 35 mm In distribution
213-89-00 In distribution
209-04-75 SIZE 5 In distribution
02-019-10-0240 SIZE 4 In distribution
201-13-15 Angle 5 ° In distribution
209-56-12 Outer Diameter 12 mm In distribution
205-75-03 SIZE 3 In distribution
213-56-53 SIZE 3.5 In distribution
213-50-11 SIZE 1 In distribution
02-019-50-0340 SIZE 4 In distribution
213-53-00 SIZE 0 In distribution
205-75-01 SIZE 1 In distribution
201-13-07 In distribution
213-53-11 SIZE 1 In distribution
205-56-03 Outer Diameter 15 mm In distribution
213-64-29 Width 29 mm In distribution
02-029-21-8110 In distribution
201-50-00 Outer Diameter 4 mm In distribution
213-56-52 SIZE 2.5 In distribution
213-50-10 SIZE 0 In distribution
205-56-06 Outer Diameter 21 mm In distribution
207-49-00 In distribution
207-48-20 1/8″ Pegs In distribution
201-51-78 SIZE 3.5 In distribution
02-019-70-0001 In distribution
213-65-53 Lumen/Inner Diameter 53 mm In distribution

Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy® Microport Orthopedics Inc. 4,423
Exult Knee Replacement System Corentec Co., Ltd. 1,770
Freedom Maxx Orthopedics Inc. 1,693
Legion Smith & Nephew, Inc. 1,534
MyKnee Medacta International SA 1,466
Journey Smith & Nephew, Inc. 1,339
Persona® Zimmer, Inc. 1,254
DJO Surgical Encore Medical, L.P. 1,131
U2 Total Knee System United Orthopedic Corp. 1,078
CKS Plus Shalby Advanced Technologies, Inc. 1,024
Lospa Modular Knee System Corentec Co., Ltd. 1,020
Natural-Knee® Zimmer, Inc. 980

Showing 12 of 1,175. All products under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K223252 2023-07-17
K171045 2017-04-28
K170240 2017-02-23
K153595 2016-03-25
K160484 2016-03-18
K152170 2015-09-03
K150890 2015-05-29
K132161 2013-10-11
K123687 2013-03-20
K123342 2013-01-10
K121307 2012-05-31
K111400 2011-07-28
K101981 2010-08-02
K093360 2010-01-11
K082022 2008-09-02
K071738 2007-08-15
K032522 2004-05-28
K033883 2004-02-13
K032606 2003-09-23
K030686 2003-04-02
K023186 2002-10-17
K012251 2001-07-31
K011976 2001-07-16
K010434 2001-03-13
K954208 1996-02-26
K933494 1995-03-10
K932690 1995-02-09
K933610 1995-01-17
K935773 1994-12-09
K932776 1994-10-20
K935726 1994-10-20
K936079 1994-09-07

Recalls Naming This Product

59 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Exactech, Inc. 510(k) number 2024-04-18 Class II Under Investigation by firm Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.
Exactech, Inc. 510(k) number 2024-04-18 Class II Under Investigation by firm Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.
Exactech, Inc. 510(k) number 2024-04-18 Class II Under Investigation by firm Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.
Exactech, Inc. 510(k) number 2024-04-18 Class II Under Investigation by firm Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.
Exactech, Inc. 510(k) number 2023-11-21 Class II Packaging change control Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Exactech, Inc. 510(k) number 2023-11-21 Class II Packaging change control Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Exactech, Inc. 510(k) number 2023-11-21 Class II Packaging change control Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Exactech, Inc. 510(k) number 2023-11-21 Class II Packaging change control Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
Exactech, Inc. 510(k) number 2022-08-11 Class II Process control Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear. 7946 devices
Exactech, Inc. 510(k) number 2021-08-30 Class II Process control Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. 242,397 devices
Exactech, Inc. 510(k) number 2021-08-30 Class II Process control Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. 109,787 devices
Exactech, Inc. 510(k) number 2021-08-30 Class II Process control Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. 31,201 devices
Exactech, Inc. 510(k) number 2020-01-27 Class II Labeling mix-ups These Truliant Splined Stem Extension, 18mm x 120mm were found to have a labeling error. The upper right corner of the label incorrectly identifies the implant size as 17mm x 80mm when the implant size is 18mm x 120mm. 4 units
Exactech, Inc. 510(k) number 2018-05-08 Class II Under Investigation by firm Potentially have non-conforming internal threads. 1
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 57 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 109 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 114 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 198 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 207 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 640 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 665 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 801 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 893 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 733 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 683 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 720 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 527 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 573 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 547 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 537 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 311 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 333 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 317 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 306 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 643 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 840 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 889 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 920 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 953 devices 2021-06-21
Exactech, Inc. 510(k) number 2017-09-19 Class II Labeling design There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. 895 devices 2021-06-21

Showing 40 of 59.

Recalls

6 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2023-11-21 Class II Packaging change control Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
2021-08-30 Class II Process control Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. 33,103 devices
2021-08-30 Class II Process control Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. 12 devices
2021-08-30 Class II Process control Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. 8,985 devices
2021-08-30 Class II Process control Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. 41 devices
2019-03-13 Class II Under Investigation by firm 2.5 Truliant Fit Trays were mismarked as 3 18 units 2021-04-22

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer