510(k) K120686 ยท HCG Device, Neurovascular Embolization
ORBIT GALAXY G2 MICROCOIL DELIVERY SYSTEM
| Applicant | Codman & Shurtleff, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Apr 4, 2012 |
| Received | Mar 6, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120686
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.