K070015 is an FDA 510(k) clearance for the COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT. This device is classified as a Bone Cement (Class II - Special Controls, product code LOD).
Submitted by Biomet Manufacturing Corp (Warsaw, US). The FDA issued a Cleared decision on November 30, 2007, 331 days after receiving the submission on January 3, 2007.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3027.
| 510(k) Number | K070015 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 03, 2007 |
| Decision Date | November 30, 2007 |
| Days to Decision | 331 days |
| Submission Type | Abbreviated |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | LOD — Bone Cement |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3027 |