510(k) K934582 ยท KWP Appliance, Fixation, Spinal Interlaminal
GDLH VARIABLE ANGLE CONNECTOR
| Applicant | Danek Group, Inc., Memphis TN, US |
| Decision | Substantially Equivalent for Some Indications, Jun 21, 1994 |
| Received | Sep 23, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934582
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.