FDA 510(k) Applications Submitted by PRAESIDIA S.R.L.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K063009 | 10/02/2006 | FLEXIGRIP STERNAL CLOSURE SYSTEM, MODEL FG0200 THROUGH FG0400 (NONE SIZES) | PRAESIDIA S.R.L. |
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