510(k) K122509 ยท KWP Appliance, Fixation, Spinal Interlaminal
VERTIFLEX SPINOUS PROCESS FIXATION PLATE
| Applicant | Vertiflex, Inc., San Clamente CA, US |
| Decision | Substantially Equivalent, Dec 17, 2012 |
| Received | Aug 17, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122509
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.