Global Ap 1130-52-500
Global Ap 1130-52-500 (113052500) 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 10603295006220), 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 | Number10603295006220 | Date24 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK060874 | Date28 Jun 2006 | StatusActive |
Official records
- AccessGUDID record 10603295006220
- FDA 510(k) database K060874
Across registries
- FDA 510(k) K060874 decided 28 Jun 2006 Active
- FDA GUDID UDI-DI 10603295006220 listed 24 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K060874
- Listed FDA GUDID 10603295006220
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Global Ap
- Generic name
- Stem-fixed metallic humeral head prosthesis
- Model / Ref / Catalog
- 1130-52-500, 113052500
- Primary DI / UDI-DI
- 10603295006220
- 510(k) Number
- FDA product code
- HSD, KWS
- GMDN term
- Stem-fixed metallic humeral head prosthesis
- Device class
- Class II
- Regulation number
- 888.3690, 888.3660
- GUDID distribution status
- In Commercial Distribution
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