Clearance Summary
OPUS MAGNUM ANCHOR & INSTRUMENT SET received FDA 510(k) clearance under submission number K020172, sponsored by Opus Medical, 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 2002-07-22.
- Submission: K020172
- Applicant / Sponsor: Opus Medical, Inc.
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2002-07-22
Classification & Regulation
This clearance is catalogued under FDA product code MBI and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.