510(k) K072187 ยท MNI Orthosis, Spinal Pedicle Fixation
PIONEER LOWTOP SPINAL ROD SYSTEM
| Applicant | Pioneer Surgical Technology, Marquette MI, US |
| Decision | Substantially Equivalent, Oct 12, 2007 |
| Received | Aug 6, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072187
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.