510(k) K101762 ยท MRW System, Facet Screw Spinal Device
VIPER F2 FACET FIXATION SYSTEM
| Applicant | Depuy Spine, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Nov 15, 2010 |
| Received | Jun 22, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101762
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.