510(k) K991862 ยท MNI Orthosis, Spinal Pedicle Fixation
MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS)
| Applicant | Micomed GmbH, Fullerton CA, US |
| Decision | Substantially Equivalent, Jan 13, 2000 |
| Received | Jun 1, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991862
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.