510(k) K021275 ยท MNI Orthosis, Spinal Pedicle Fixation
MICOMED POSTERIOR DOUBLEROD SYSTEM
| Applicant | Micomed Ortho GmbH, Lake Forest CA, US |
| Decision | Substantially Equivalent, Jul 18, 2002 |
| Received | Apr 22, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021275
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.