510(k) K013829 ยท MRW System, Facet Screw Spinal Device
MODIFICATION TO TOWNLEY TRANSFACETPEDICULAR SCREW FIXATION SYSTEM
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Dec 19, 2001 |
| Received | Nov 19, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013829
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.