510(k) K021705 ยท MRW System, Facet Screw Spinal Device
MODIFICATION TO TOWNLEY TRANSFACEPEDICULAR SCREW FIXATION SYSTEM
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jul 24, 2002 |
| Received | May 23, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021705
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.