Clearance Summary
COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT received FDA 510(k) clearance under submission number K070015, sponsored by Biomet Manufacturing Corp. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-11-30.
- Submission: K070015
- Applicant / Sponsor: Biomet Manufacturing Corp
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3027
- Decision date: 2007-11-30
Classification & Regulation
This clearance is catalogued under FDA product code LOD and 21 CFR 888.3027, within the Orthopedic review panel as a Class II device.