Clearance Summary
MICROLOC(TM) POROUS COATED UNICONDYLAR KNEE SYSTEM received FDA 510(k) clearance under submission number K880826, sponsored by Johnson & Johnson Professionals, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1988-03-14.
- Submission: K880826
- Applicant / Sponsor: Johnson & Johnson Professionals, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3500
- Decision date: 1988-03-14
Classification & Regulation
This clearance is catalogued under FDA product code KYK and 21 CFR 888.3500, within the Orthopedic review panel as a Class II device.