510(k) K070229 ยท MNI Orthosis, Spinal Pedicle Fixation
RANGE SPINAL SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, May 3, 2007 |
| Received | Jan 24, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070229
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.