FDA 510(k) Applications Submitted by JILL YELTON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K093361 | 10/28/2009 | SYNTHES AIR PEN DRIVE (APD) SYSTEM | SYNTHES (USA) |
| K090658 | 03/12/2009 | SYNTHES EXTERNAL FIXATION DEVICES, MR CONDITIONAL | SYNTHES (USA) |
| K092190 | 07/21/2009 | SYNTHES DISTRACTION OSTEOGENESIS SYSTEM, MR CONDITIONAL WITH EXPANDED INDICATIONS | SYNTHES (USA) |
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