Cemex System Fast 40g

Cemex System Fast 40g is a polymethylmethacrylate bone cement with a fast setting. Cemex System Fast 40g holds the powder (40g) and liquid (16,7g) components separately within a closed…

Registry build 21.09.26

Cemex System Fast 40g is a polymethylmethacrylate bone cement with a fast setting. Cemex System Fast 40g holds the powder (40g) and liquid (16,7g) components separately within a closed syringe-like device that serves as both a mixing chamber and a cement delivery system. The device is supplied sterile, for single use. Cemex System Fast 40g is indicated for the fixation of joint prosthesis implants to the host bone.

1manufacturer
1catalogue number

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 Cemex System Fast 40G
Listed by Tecres SPA, Italy
FDA product code LOD
Device type Bone Cement
Device class Class 2
Regulation 21 CFR 888.3027
Establishment Contract manufacturer, Manufacturer, Exporter
510(k) K031430
Record published 2015-10-07
Record revised 2018-07-06 (version 3)

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

Catalogue Numbers

Catalogue numbers for Cemex System Fast 40G
Catalogue number Size Status
13A2020 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
Bone Cement Depuy (Ireland) 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

Showing 12 of 63. All products under Bone Cement

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