Libertas MO-MLUH-MK/32
Libertas MO-MLUH-MK/32 is a Class II device made by Maxx Orthopedics Inc., cleared under FDA 510(k) K180973 on 28 Sep 2018 and listed in FDA GUDID since 29 Jul 2025 (UDI-DI 00810008125366), 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 | GUDID listing | Number00810008125366 | Date29 Jul 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK180973 | Date28 Sep 2018 | StatusActive |
Official records
- AccessGUDID record 00810008125366
- FDA 510(k) database K180973
Across registries
- FDA 510(k) K180973 decided 28 Sep 2018 Active
- FDA GUDID UDI-DI 00810008125366 listed 29 Jul 2025 Listed
Timeline
- Cleared FDA 510(k) K180973
- Listed FDA GUDID 00810008125366
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Libertas
- Generic name
- Metal-on-polyethylene total hip prosthesis
- Model / reference
- MO-MLUH-MK/32
- Primary DI / UDI-DI
- 00810008125366
- 510(k) Number
- FDA product code
- LZO
- GMDN term
- Metal-on-polyethylene total hip prosthesis
- Device class
- Class II
- Regulation number
- 888.3353
- GUDID distribution status
- In Commercial Distribution