510(k) K033352 ยท MNI Orthosis, Spinal Pedicle Fixation
VERTEBRON PSS PEDICLE SCREW SYSTEM
| Applicant | Vertebron, Inc., Stratford CT, US |
| Decision | Substantially Equivalent, Feb 25, 2004 |
| Received | Oct 20, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033352
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.