Clearance Summary
CORIN TRINITY-I ACETABULAR SHELL received FDA 510(k) clearance under submission number K122305, sponsored by Corin USA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-11-21.
- Submission: K122305
- Applicant / Sponsor: Corin USA
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3353
- Decision date: 2012-11-21
Classification & Regulation
This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.