Clearance Summary
STALIF (TM) C received FDA 510(k) clearance under submission number K072415, sponsored by Surgicraft , Ltd.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-01-25.
- Submission: K072415
- Applicant / Sponsor: Surgicraft , Ltd.
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3080
- Decision date: 2008-01-25
Classification & Regulation
This clearance is catalogued under FDA product code OVE and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.