510(k) K071457 ยท MMX Device, Percutaneous Retrieval
MODIFICATION TO RADIUS SNARE
| Applicant | Radius Medical Technologies, Inc., Acton MA, US |
| Decision | Substantially Equivalent, Sep 25, 2007 |
| Received | May 25, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071457
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.