510(k) K020134 ยท KWP Appliance, Fixation, Spinal Interlaminal
SPIRAL RADIUS 90-D RODDING SYSTEM
| Applicant | United States Surgical, A Division of Tyco Healthc, Norwalk CT, US |
| Decision | Substantially Equivalent, Apr 15, 2002 |
| Received | Jan 15, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020134
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.