510(k) K060121 ยท HAW Neurological Stereotaxic Instrument
BIOMET PRE-CALIBRATED COMPUTER AIDED SURGERY NAVIGATION INSTRUMENTS FOR HIP APPLICATIONS
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Mar 21, 2006 |
| Received | Jan 17, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060121
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.