Clearance Summary
GMK REVISION KNEE SC LINERS received FDA 510(k) clearance under submission number K103170, sponsored by Medacta International S.A.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-03-24.
- Submission: K103170
- Applicant / Sponsor: Medacta International S.A.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3560
- Decision date: 2011-03-24
Classification & Regulation
This clearance is catalogued under FDA product code JWH and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.