K234044
- 510(k) number
- K234044
- Device name
- ACS® LD FB Knee System
- Applicant
- Implantcast GmbH DE
- Product code
- JWH — Prosthesis, Knee, Patellofemorotibial, Semi-Constrai
- Decision date
- 2024-09-06
- Date received
- 2023-12-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K234044.pdf
Official FDA record: K234044
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.