Bone Cement

DEPUY CMW 2 GENTAMICIN Fast Set Bone Cement 20g

Registry build 21.09.26
1manufacturer
5catalogue numbers in this listing

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code LOD
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for Bone Cement
Listed by Depuy (Ireland), Ireland
FDA product code LOD
Device type Bone Cement
Device class Class 2
Regulation 21 CFR 888.3027
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K023103
Record published 2015-09-24
Record revised 2020-06-19 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Handling environment temperature up to 25 °C; Storage environment temperature up to 25 °C
Packaging Package of 10, case of 20

Catalogue Numbers

Catalogue numbers for Bone Cement
Catalogue number Size Status
5450-31-500 In distribution
3312-040 In distribution
3332-040 In distribution
5450-32-500 In distribution
3322-020 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Palacos Heraeus Medical LLC 17
Kiva Benvenue Medical, Inc. 6
Rally Smith & Nephew, Inc. 5
PCD SpinePlex Stryker GmbH 4
Simplex Howmedica Osteonics Corp 4
DJO Surgical Encore Medical, L.P. 4
Gentafix Teknimed SAS 3
Versabond Smith & Nephew, Inc. 3
Orthoset® Microport Orthopedics Inc. 3
Osteopal® Heraeus Medical LLC 3
Prostalac Depuy Orthopaedics, Inc. 3
Signature -x Cement Teknimed SAS 3

Showing 12 of 63. All products under Bone Cement

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Bone Cement
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Depuy Orthopaedics, Inc. 510(k) number 2015-02-11 Class II Under Investigation by firm One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated. This may result in surgical delays while a replacement package of cement is retrieved and mixed. 1267 2015-05-19

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P970010 2000-08-31 NORIAN SRS BONE CEMENT Synthes (Usa)
P960001 1999-08-26 DEPUY 3 BONE CEMENT Depuy Intl., Ltd.
N18466 1998-10-21 ORTHOSET BONE CEMENT Depuy Intl., Ltd.
N17004 1996-12-18 SURGICAL SIMPLEX(R) P RADIOPAQUE BONE CEMENT Howmedica Corp.
N17003 1993-06-08 SURGICAL SIMPLEX(R) P BONE CEMENT Howmedica Corp.
P810020 1992-02-14 PALACOS R BONE CEMENT Smith & Nephew Richards, Inc.
N17755 1990-08-02 BONECEMENT Zimmer, Inc.
N17113 1981-09-16 OMNIPLASTIC BONE CEMENT L.D. Caulk Co.

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