510(k) K990303 ยท KWP Appliance, Fixation, Spinal Interlaminal
EBI OMEGA 21 SYSTEM
| Applicant | Electro-Biology, Inc., Parsippany NJ, US |
| Decision | Substantially Equivalent, Apr 29, 1999 |
| Received | Feb 1, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990303
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.