Ascent Knee System 179022
Ascent Knee System 179022 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K982869 on 22 Sep 1998 and listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00880304261945), 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 | Number00880304261945 | Date24 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK982869 | Date22 Sep 1998 | StatusActive |
Official records
- AccessGUDID record 00880304261945
- FDA 510(k) database K982869
Across registries
- FDA 510(k) K982869 decided 22 Sep 1998 Active
- FDA GUDID UDI-DI 00880304261945 listed 24 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K982869
- Listed FDA GUDID 00880304261945
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ascent Knee System
- Generic name
- Uncoated knee femur prosthesis, metallic
- Model / Ref / Catalog
- 179022
- Primary DI / UDI-DI
- 00880304261945
- 510(k) Number
- FDA product code
- JWH
- GMDN term
- Uncoated knee femur prosthesis, metallic
- Device class
- Class II
- Regulation number
- 888.3560
- GUDID distribution status
- In Commercial Distribution
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