Zimmer Patient Specific Instruments

NexGen® CR-FLEX PIN GUIDES (FEMUR AND TIBIA) CT

Registry build 21.09.26
12manufacturers in China registered for this device type
8catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MBH
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
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
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
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for Zimmer Patient Specific Instruments
Listed by Materialise NV, Belgium
FDA product code MBH
Device type Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3565
510(k) K113829
Record published 2017-07-21
Record revised 2019-11-27 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Distribution end date 2019-03-01

Catalogue Numbers

Catalogue numbers for Zimmer Patient Specific Instruments
Catalogue number Size Status
00-5970-000-17 Withdrawn
00-5970-000-03 Withdrawn
00-5970-000-16 Withdrawn
00-5970-000-18 Withdrawn
00-5970-000-36 Withdrawn
00-5970-000-15 Withdrawn
00-5970-000-33 Withdrawn
00-5970-000-19 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy Microport Orthopedics Inc. 4,272
Triathlon Howmedica Osteonics Corp 712
Instrument Howmedica Osteonics Corp 709
Persona® Vivacit-E® Zimmer, Inc. 499
Arthrex® Arthrex, Inc. 494
Persona® Zimmer, Inc. 441
Legion Smith & Nephew, Inc. 397
U2 Total Knee System United Orthopedic Corp. 286
Attune Depuy (Ireland) 234
DJO Surgical Encore Medical, L.P. 191
Vanguard XP Instrumentation Biomet Orthopedics 150
Truliant® Exactech, Inc. 142

Showing 12 of 948. All products under Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K140257 2014-04-02
K093533 2010-02-17

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