Clearance Summary
HI-FI ULTRAFIX KNOTLESS MINIMITE SUTURE ANCHOR received FDA 510(k) clearance under submission number K060714, sponsored by Conmed Linvatec. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-04-06.
- Submission: K060714
- Applicant / Sponsor: Conmed Linvatec
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2006-04-06
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.