Agility 1555-06-030
Agility 1555-06-030 (155506030) is a Class II device made by Depuy Orthopaedics, Inc., cleared under FDA 510(k) K020541 on 20 May 2002 and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 10603295058625), 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 | Number10603295058625 | Date24 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK020541 | Date20 May 2002 | StatusActive |
Official records
- AccessGUDID record 10603295058625
- FDA 510(k) database K020541
Across registries
- FDA 510(k) K020541 decided 20 May 2002 Active
- FDA GUDID UDI-DI 10603295058625 listed 24 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K020541
- Listed FDA GUDID 10603295058625
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Agility
- Generic name
- Coated ankle talus prosthesis
- Model / Ref / Catalog
- 1555-06-030, 155506030
- Primary DI / UDI-DI
- 10603295058625
- 510(k) Number
- FDA product code
- HSN
- GMDN term
- Coated ankle talus prosthesis
- Device class
- Class II
- Regulation number
- 888.3110
- GUDID distribution status
- In Commercial Distribution