FDA 510(k) Applications Submitted by HANDE TUFAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080568 | 02/29/2008 | X-MESH EXPANDABLE CAGE SYSTEM | DEPUY SPINE, INC. |
| K081432 | 05/21/2008 | HEALOS II BONE GRAFT SUBSTITUTE | DEPUY SPINE, INC. |
| K081758 | 06/20/2008 | HEALOS FX INJECTABLE BONE GRAFT REPLACEMENT, MODELS 276175002, 276175005, 276175010, 276175015 | DEPUY SPINE, INC. |
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