510(k) K130235 ยท NUN Bone Grafting Material, Human Source
SURFUSE II GEL, SURFUSE II PUTTY, EXFUSE II GEL, EXFUSE II PUTTY
| Applicant | Hans Biomed Corp., Chevy Chase MD, US |
| Decision | Substantially Equivalent, Jan 10, 2014 |
| Received | Jan 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130235
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.