Instrument

Exeter Plug Spare Adapter FOR Plug DIA 10-12-14-16-18-20MM (Spare Part)

Registry build 21.09.26
13manufacturers in China registered for this device type
167catalogue numbers in this listing
17510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Zhejiang (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JDI
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
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54

Showing 12 of 13. All 13 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Record

Regulatory record for Instrument
Listed by Howmedica Osteonics Corp, United States
FDA product code JDI
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device class Class 2
Regulation 21 CFR 888.3350
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
510(k) K173499
Record published 2018-05-03
Record revised 2024-05-10 (version 9)

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
Packaging Pack of 25, pack of 10
Sizes Lumen/inner diameter 22 to 46 mm; length 2 to 150 mm; outer diameter 36 to 64 mm
Distribution end date 2023-10-02
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Instrument
Catalogue number Size Status
0585-9-502 Offset: 50.0 Millimeter In distribution
1601-1009A Size: 9 In distribution
I-H2125NT37 Offset: 37.5 Millimeter In distribution
1030-1250 In distribution
1020-5206 Size: 6 In distribution
2102-0468 Diameter: 68.0 Millimeter In distribution
I-H21103625 Diameter: 36.0 Millimeter In distribution
2102-0438 Diameter: 38.0 Millimeter In distribution
I-H1282H040 Offset: -4.0 Millimeter In distribution
1090-2854 Diameter: 54.0 Millimeter In distribution
6264-8-828R Offset: 5.0 Millimeter In distribution
1235-0-582 Outer Diameter 58.0 mm In distribution
2124-1700 Side: RIGHT In distribution
1235-0-014A In distribution
I-H1282H140 Offset: 0.0 Millimeter In distribution
I-H2108PL58 Diameter: 58.0 Millimeter In distribution
2208-4060 Diameter: 60.0 Millimeter In distribution
2250-36I Degree: 10.0 Degree In distribution
0930-3-005 Taper Connection: V40? In distribution
I-H0985HA0H Alpha Code: H In distribution
6060-5-310 In distribution
2200-40J Degree: 0.0 Degree In distribution
2102-0003 In distribution
1150-2354 Outer Diameter 54.0 mm In distribution
2250-28D Degree: 10.0 Degree In distribution
1100-3600R Offset: 0.0 Millimeter In distribution
6825-9-945 Outer Diameter 45.0 mm In distribution
I-H1387H46D Diameter: 46.0 Millimeter In distribution
0581-1-441 Taper Connection: V40? In distribution
I-H20213230 Degree: 132.0 Degree In distribution
7002-0141 Diameter: 41.0 Millimeter In distribution
7003-0000 In distribution
I-H2022AG00 In distribution
1150-2364 Outer Diameter 64.0 mm In distribution
2199-2028 Diameter: 28.0 Millimeter In distribution
I-H0929H324 Offset: 8.0 Millimeter In distribution
1100-4497R Offset: -2.5 Millimeter In distribution
2111-3022 Diameter: 22.0 Millimeter In distribution
6825-9-941 Outer Diameter 41.0 mm In distribution
I-H1288HA0C Alpha Code: C In distribution
I-H0929H361 Offset Standard: Standard In distribution
5260-6-300 In distribution
1020-5207 Size: 7 In distribution
0585-9-441 Offset: 44.0 Millimeter In distribution
2240-36I Degree: 0.0 Degree In distribution
I-H0929H281 Offset: -4.0 Millimeter In distribution
0585-9-503 Size: 3 In distribution
I-H1282HF13 Taper Connection: V40? In distribution
0585-9-374 Length 150.0 mm In distribution
1020-5201 Size: 1 In distribution
1113-1002 Size: Standard In distribution
I-H1387H50E Diameter: 50.0 Millimeter In distribution
0585-9-351 Offset: 35.5 Millimeter In distribution
6264-8-126R Taper Connection: V40? In distribution
2200-26J Alpha Code: J In distribution
2250-28E Alpha Code: E In distribution
I-H19660110 Diameter: 10.0 Millimeter In distribution
I-H2108ER54 Diameter: 54.0 Millimeter In distribution
I-H2108ER50 Diameter: 50.0 Millimeter In distribution
I-H20212725 Neck Length: 25.0 Millimeter In distribution
1212-0016 Length 16.0 mm In distribution
I-H21103605 Offset: -5.0 Millimeter In distribution
I-H0929H321 Offset Standard: Standard In distribution
1020-2300 In distribution
2112-0010 In distribution
1100-2825R Taper Connection: C-TPR In distribution
I-H0929H221 Diameter: 22.0 Millimeter In distribution
I-H0929H286 Offset: 16.0 Millimeter In distribution
1030-3250 Outer Diameter 50.0 mm In distribution
I-H2108PR56 Diameter: 56.0 Millimeter In distribution
7002-0142 Diameter: 42.0 Millimeter In distribution
2102-0437 Diameter: 37.0 Millimeter In distribution
I-H19660118 Diameter: 18.0 Millimeter In distribution
2200-22B Alpha Code: B In distribution
I-H21103204 Offset: -4.0 Millimeter In distribution
0581-1-444 Size: 4 In distribution
2250-36E Degree: 10.0 Degree In distribution
7002-0144 Diameter: 44.0 Millimeter In distribution
I-H1387H52E Diameter: 52.0 Millimeter In distribution
I-H1288HA0B Alpha Code: B In distribution
2208-2074A Diameter: 74.0 Millimeter In distribution
I-H0985HA0E Alpha Code: E In distribution
1020-5210 Size: 10 In distribution
I-H1855BH01 Size: 1 In distribution
2250-32G Degree: 10.0 Degree In distribution
1030-2252 Lumen/Inner Diameter 22.0 mm In distribution
I-H2125NT50 Offset: 50.0 Millimeter In distribution
7002-0159 Diameter: 59.0 Millimeter In distribution
0585-9-440 Offset: 44.0 Millimeter In distribution
2200-36D Alpha Code: D In distribution
2210-22A Alpha Code: A In distribution
I-H1855BH06 Size: 6 In distribution
0581-1-330 Offset: 33.0 Millimeter In distribution
I-H1855BH11 Size: 11 In distribution
7002-0147 Diameter: 47.0 Millimeter In distribution
2270-32J Diameter: 32.0 Millimeter In distribution
0581-1-440 Size: 0 In distribution
2240-28E Lumen/Inner Diameter 28.0 mm In distribution
0939-2-000 In distribution
2102-0473 Diameter: 73.0 Millimeter In distribution
I-H1282HF07 Offset: 8.0 Millimeter In distribution
1020-2200 Size: SM In distribution
1601-34132 Degree: 132.0 Degree In distribution
6842-6-105 Taper Connection: V40? In distribution
1110-0406 In distribution
1235-0-858 In distribution
1100-4097R Head Diameter: 40.0 Millimeter In distribution
1235-C-0030 Taper Connection: C-TPR In distribution
I-H1862HB07 Size: 7 In distribution
I-H1855BH07 Size: 7 In distribution
1020-1200 In distribution
1212-0017 Length 17.0 mm In distribution
1235-0-003 In distribution
0585-9-210 In distribution
I-H1282HF01 Offset: 7.5 Millimeter In distribution
7002-0167 Diameter: 67.0 Millimeter In distribution
6278-8-311 Diameter: 11.0 Millimeter In distribution
I-H19660112 Diameter: 12.0 Millimeter In distribution
I-H1387H60G Diameter: 60.0 Millimeter In distribution
I-H1862HB08 Size: 8 In distribution
0585-9-561 Offset: 56.0 Millimeter In distribution
0581-1-562 Offset: 56.0 Millimeter In distribution
2208-6063R Outer Diameter 63.0 mm In distribution
1030-2846 Lumen/Inner Diameter 28.0 mm In distribution
I-H0929H325 Diameter: 32.0 Millimeter In distribution
I-H1282H340 Offset: 8.0 Millimeter In distribution
2250-36H Degree: 10.0 Degree In distribution
1601-1007A Size: 7 In distribution
I-H1387H58G Diameter: 58.0 Millimeter In distribution
1235-0-242 Outer Diameter 36.0 mm In distribution
0585-9-373 Size: 3 In distribution
0932-2-000 Size: LGE In distribution
1601-1012A Size: 12 In distribution
0580-3744-0 Offset: 44.0 Millimeter In distribution
I-H19660301 Side: RIGHT In distribution
I-H2125NT44 Offset: 44.0 Millimeter In distribution
6264-8-326R Offset: 8.0 Millimeter In distribution
1235-0-602 Outer Diameter 60.0 mm In distribution
7002-0149 Diameter: 49.0 Millimeter In distribution
1235-0-860 In distribution
I-H19660200 In distribution
3200-46F Alpha Code: F In distribution
2240-32H Degree: 0.0 Degree In distribution
6278-8-328 Diameter: 28.0 Millimeter In distribution
7002-0153 Diameter: 53.0 Millimeter In distribution
0580-355-0 Size: 0 In distribution
1235-0-621 Outer Diameter 62.0 mm In distribution
1100-4075R Head Diameter: 40.0 Millimeter In distribution
I-H1236HA01 Length 2.0 mm Withdrawn
I-H0789HA40 Length 40.0 mm Withdrawn
I-H10043360 Diameter: 3.3 Millimeter Withdrawn
I-H0659HA67 Diameter: 67.0 Millimeter Withdrawn
I-H1157132D Alpha Code: D Withdrawn
I-H0659HA61 Diameter: 61.0 Millimeter Withdrawn
I-H0659HA44 Diameter: 44.0 Millimeter Withdrawn
I-H0659HA58 Diameter: 58.0 Millimeter Withdrawn
I-H08452059 Diameter: 59.0 Millimeter Withdrawn
I-H08452049 Diameter: 49.0 Millimeter Withdrawn
I-H20212735 Taper Connection: C-TPR Withdrawn
I-H0978HA00 Withdrawn
I-H0659HA59 Diameter: 59.0 Millimeter Withdrawn
I-H1004HA16 Length 16.0 mm Withdrawn
I-H0659HA66 Diameter: 66.0 Millimeter Withdrawn
I-H1961H364 Taper Connection: V40? Withdrawn
I-H0669HA36 Diameter: 36.0 Millimeter Withdrawn
I-H0921HA00 Withdrawn
I-H0659HA75 Diameter: 75.0 Millimeter Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Zimmer, Inc. 836
R3 Smith & Nephew, Inc. 497
UniSyn Hip System Shalby Advanced Technologies, Inc. 247
UniSyn® Hip System Consensus Orthopedics, Inc. 247
Reflection Smith & Nephew, Inc. 170
Echelon Smith & Nephew, Inc. 159
B-P Total HIP System Endotec, Inc. 151
ZCA® Zimmer, Inc. 149
Omnifit Howmedica Osteonics Corp 149
Ringloc HIP System Biomet Orthopedics 139
Profemur Microport Orthopedics Inc. 113
OSS™ Orthopedic Salvage System Biomet Orthopedics 98

Showing 12 of 444. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K193429 2020-08-13
K120578 2012-03-29
K110290 2011-09-27
K052748 2005-12-02
K051363 2005-06-23
K050138 2005-03-21
K031730 2003-08-29
K031744 2003-08-08
K022799 2002-11-21
K022077 2002-07-25
K021310 2002-05-21
K020989 2002-04-26
K012026 2001-07-18
K011623 2001-06-15
K010757 2001-04-11
K010310 2001-03-20
K001956 2000-12-11

Recalls Naming This Product

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

Recalls naming the identifiers of Instrument
Recalled by Identified by Initiated FDA class Root cause Reason
Howmedica Osteonics Corp 510(k) number 2021-10-15 Class II Under Investigation by firm XXX
Howmedica Osteonics Corp 510(k) number 2021-10-15 Class II Under Investigation by firm There is a potential for the outer white Tyvek lid to debond from the sealed package.

Recalls

18 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
2025-08-28 Class II Under Investigation by firm a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted. 55 units (all OUS)
2024-08-05 Class II Process control A patient specific, custom-made device was supplied for a surgical procedure that did not match the design proposal. 1 unit (OUS only)
2019-11-07 Class II Employee error May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire 20 units 2020-08-31
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2016-08-29 Class II Under Investigation by firm Stryker received several complaints describing incidence of harm secondary to taper lock failure for specific lots of numerous catalog numbers of LFIT Anatomic CoCr V40 Femoral Heads. 42,519 units (total Catalog numbers) 2017-05-02
2016-07-01 Class II Device Design Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle. 241 units 2017-06-08
2015-10-15 Class II Under Investigation by firm Six (6) PCA 10 Degree Hooded Acetabular Insert-Duration 22 mm (ID) have been distributed in the US, although the 22 mm size was inadvertently omitted from 510(k) #K963612. 1 unit 2017-06-08
2015-02-03 Class II Under Investigation by firm Three customer complaints were received for the same batch of V40 LFIT Vitallium femoral heads (part number 6260-9-032, lot 48681201) alleging that the femoral head couldn’t be assembled with its corresponding V40 stem trunnion. 9 units 2017-04-07
2013-10-25 Class II Packaging process control Stryker received a report from the field indicating that an Accolade II Hip Stem Size #3 was identified in packaging with an Accolade II Hip Stem Size #5. 20 units 2015-03-31
2012-07-16 Class II Device Design Stryker has become aware that insufficient taper torsional strength may result when a PAR extension piece is used with a forged CoCr stem. 301 units 2015-09-09
2011-12-29 Class II Employee error Stryker Orthopaedics has become aware of the potential for cracking of the PMMA coating on their PM COCR Hip Stem product. 16,913 units 2015-03-19
2010-03-31 Not classified Process control One lot of 13 mm medium distal ring centralizers and 14 mm large distal ring centralizer have been labeled incorrectly. The size 14 Large centralizers have been labeled as size 13 Medium centralizers and size 13 Medium centralizers have bee 17 2010-07-09
2010-03-31 Not classified Process control One lot of 13 mm medium distal ring centralizers and 14 mm large distal ring centralizer have been labeled incorrectly. The size 14 Large centralizers have been labeled as size 13 Medium centralizers and size 13 Medium centralizers have bee 15 2010-07-09
2010-03-29 Not classified Error in labeling Stryker became aware that device labels have incorrectly printed manufacture dates and thus incorrect expiration dates on the product label. 24 units 2012-09-10
2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
2007-12-18 Not classified Labeling design The GMRS Proximal Femoral Surgical Protocol states ” The GMRS Proximal Femoral components are fully compatabile with all Stryker V40 femoral heads.” This statement is incorrect and conflicts with the Alumina Head label and packaging insert 5869 2008-10-15
2007-11-15 Not classified Process design Curvature Discrepancy –The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy –The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-02 Not classified Other Fracture of Stem Neck – The firm recently performed laboratory testing indicates that there may be a potential increased risk of stem neck fractures when a V40 +16mm offset femoral head is mated with certain Accolade TMZF femoral stems in p 5,599 total units 2010-08-30
2007-11-02 Not classified Other Fracture of Stem Neck – The firm recently performed laboratory testing indicates that there may be a potential increased risk of stem neck fractures when a V40 +16mm offset femoral head is mated with certain Accolade TMZF femoral stems in p 5,599 total units 2010-08-30
2007-11-02 Not classified Other Fracture of Stem Neck – The firm recently performed laboratory testing indicates that there may be a potential increased risk of stem neck fractures when a V40 +16mm offset femoral head is mated with certain Accolade TMZF femoral stems in p 5,599 total units 2010-08-30

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