FDA 510(k) Applications Submitted by FRONTIER DEVICES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K091812 | 06/18/2009 | FRONTIER DEVICES CRANIOMAXILLOFACIAL, CRANIO CLOSURE, ORTHOGNATHIC, MANDIBLE RECONSTRUCTION AND MESH SYSTEMS | FRONTIER DEVICES, INC. |
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