Clearance Summary
MENISCUS ARROW, MODELS 531110, 531113, 531116 received FDA 510(k) clearance under submission number K993453, sponsored by Bionx Implants, Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-11-09.
- Submission: K993453
- Applicant / Sponsor: Bionx Implants, Ltd.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 1999-11-09
Classification & Regulation
This clearance is catalogued under FDA product code MAI and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.