510(k) K884585 ยท KWP Appliance, Fixation, Spinal Interlaminal
LEA PLAZA SPINAL FRAME SYSTEM
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 27, 1989 |
| Received | Nov 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884585
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.