Clearance Summary
THE MARGRON HIP REPLACEMENT SYSTEM received FDA 510(k) clearance under submission number K992815, sponsored by Portland Orthopaedics Pty. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-02-07.
- Submission: K992815
- Applicant / Sponsor: Portland Orthopaedics Pty. , Ltd.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3353
- Decision date: 2000-02-07
Classification & Regulation
This clearance is catalogued under FDA product code MEH and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.