510(k) K160991 ยท DZL Screw, Fixation, Intraosseous
Neo GBR System
| Applicant | Neobiotech Co., Ltd., Seoul, KR |
| Decision | Substantially Equivalent, Jan 10, 2017 |
| Received | Apr 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160991
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.