FDA 510(k) Applications Submitted by DARCO INTERNATIONAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061808 | 06/27/2006 | DARCO LOCKING BONE PLATE SYSTEM | DARCO INTERNATIONAL, INC. |
| K062103 | 07/24/2006 | DARCO FORCE TITANIUM COMPRESSION SCREW | DARCO INTERNATIONAL, INC. |
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