Clearance Summary
SMITH & NEPHEW HYBRID KNEE FEMORAL received FDA 510(k) clearance under submission number K042896, sponsored by Smith & Nephew, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-01-12.
- Submission: K042896
- Applicant / Sponsor: Smith & Nephew, Inc.
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3560
- Decision date: 2005-01-12
Classification & Regulation
This clearance is catalogued under FDA product code NPJ and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.