510(k) K050377 ยท HAW Neurological Stereotaxic Instrument
NBD HEAD SCREW
| Applicant | New Business Development, LLC, Woodstock GA, US |
| Decision | Substantially Equivalent, Apr 7, 2005 |
| Received | Feb 15, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050377
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.