510(k) K053160 ยท HCG Device, Neurovascular Embolization
MICRUS MODIFIED MICROCOIL 18-SYSTEM, CERECYTE, MODEL CSP & CHE
| Applicant | Micrus Endovascular Corporation, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Dec 7, 2005 |
| Received | Nov 14, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K053160
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.