FDA 510(k) Applications Submitted by PRECIMED, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K050754 | 03/23/2005 | PRECIMED CANNULATED SCREW SYSTEM | PRECIMED, INC. |
| K023851 | 11/19/2002 | PRECIMED HIP SCREW SYSTEM | PRECIMED, INC. |
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