510(k) K070245 ยท MNI Orthosis, Spinal Pedicle Fixation
CAPSURE PEDICLE SCREW SYSTEM
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Apr 5, 2007 |
| Received | Jan 25, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070245
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.