510(k) K073143 ยท MNI Orthosis, Spinal Pedicle Fixation
MODIFIED VERTIFLEX SPINAL SCREW SYSTEM
| Applicant | Vertiflex, Inc., San Clamente CA, US |
| Decision | Substantially Equivalent, Apr 7, 2008 |
| Received | Nov 7, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073143
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.