510(k) K021825 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION TO SPIRAL RADIUS 90-D SST SYSTEM
| Applicant | Unitedstates Surgical, Norwalk CT, US |
| Decision | Substantially Equivalent, Jul 1, 2002 |
| Received | Jun 4, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021825
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.