Clearance Summary
INION TRINION BIODEGRADABLE MENISCUS SCREW received FDA 510(k) clearance under submission number K031714, sponsored by Inion , 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 2004-08-16.
- Submission: K031714
- Applicant / Sponsor: Inion , Ltd.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2004-08-16
Classification & Regulation
This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.