510(k) K082267 ยท HAW Neurological Stereotaxic Instrument
PIGALILEO CAS, VERSION 4.0 AND TKR BASE, VERSION 2.1
| Applicant | Smith & Nephew, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Oct 29, 2008 |
| Received | Aug 11, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082267
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.