Cemex System Gun Application Version
510(k) K000943
Cemex System Gun Application Version is a Class II device made by Exactech, Inc., cleared under FDA 510(k) K000943 on 8 Feb 2001, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK000943 | Date8 Feb 2001 | StatusActive |
Official records
- FDA 510(k) database K000943
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LOD
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3027
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K000943
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| CEMEX SYSTEM 60G 1310/S | 1310/S | 28031497000132 | — | On the market |
| CEMEX SYSTEM 80G 1500/S | 1500/S | 28031497000217 | — | On the market |
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