Libertas MO-CCNG-58/36
Libertas MO-CCNG-58/36 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 30 Jul 2025 (UDI-DI 00840333905050), 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 | Number00840333905050 | Date30 Jul 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK180973 | Date28 Sep 2018 | StatusActive |
Official records
- AccessGUDID record 00840333905050
- FDA 510(k) database K180973
Across registries
- FDA 510(k) K180973 decided 28 Sep 2018 Active
- FDA GUDID UDI-DI 00840333905050 listed 30 Jul 2025 Listed
Timeline
- Cleared FDA 510(k) K180973
- Listed FDA GUDID 00840333905050
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Libertas
- Generic name
- Non-constrained polyethylene acetabular liner
- Model / reference
- MO-CCNG-58/36
- Primary DI / UDI-DI
- 00840333905050
- 510(k) Number
- FDA product code
- LZO
- GMDN term
- Non-constrained polyethylene acetabular liner
- Device class
- Class II
- Regulation number
- 888.3353
- GUDID distribution status
- In Commercial Distribution
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