Clearance Summary
MODIFIED ANATOMIC POROUS REPLACEMENT APR ACETABULA received FDA 510(k) clearance under submission number K850793, sponsored by Intermedics Orthopedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1985-05-09.
- Submission: K850793
- Applicant / Sponsor: Intermedics Orthopedics
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class III
- Regulation citation: 21 CFR 888.3320
- Decision date: 1985-05-09
Classification & Regulation
This clearance is catalogued under FDA product code JDL and 21 CFR 888.3320, within the Orthopedic review panel as a Class III device.