510(k) K121136 ยท KWP Appliance, Fixation, Spinal Interlaminal
RENOIR POSTERIOR CERVIAL FIXATION SYSTEM
| Applicant | Accel Spine, Dallas TX, US |
| Decision | Substantially Equivalent, Aug 9, 2012 |
| Received | Apr 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121136
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.