Global Ap 1130-06-000
Global Ap 1130-06-000 (113006000) is a Class II device made by Depuy Orthopaedics, Inc., cleared under FDA 510(k) K060874 on 28 Jun 2006 and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 10603295005445), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10603295005445 | Date24 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK060874 | Date28 Jun 2006 | StatusActive |
Official records
- AccessGUDID record 10603295005445
- FDA 510(k) database K060874
Across registries
- FDA 510(k) K060874 decided 28 Jun 2006 Active
- FDA GUDID UDI-DI 10603295005445 listed 24 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K060874
- Listed FDA GUDID 10603295005445
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Global Ap
- Generic name
- Press-fit shoulder humeral stem prosthesis
- Model / Ref / Catalog
- 1130-06-000, 113006000
- Primary DI / UDI-DI
- 10603295005445
- 510(k) Number
- FDA product code
- KWS, HSD
- GMDN term
- Press-fit shoulder humeral stem prosthesis
- Device class
- Class II
- Regulation number
- 888.3660, 888.3690
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Press-fit shoulder humeral stem prosthesis.