FDA 510(k) Applications Submitted by Robert Zoletti
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K100151 |
01/19/2010 |
APEX HIP SYSTEM BIPOLAR HEAD, MODEL H3-822XX (OD 38 TO 43MM), H3-828XX (OD44 TO 60MM) |
OMNLIFE SCIENCE |
| K071786 |
07/02/2007 |
PORTRAIT PSR |
RHYTEC INCORPORATED |
| K082197 |
08/04/2008 |
RHYTEC, INC., PORTRAIT PSR |
RHYTEC INCORPORATED |
| K072394 |
08/27/2007 |
PORTRAIT STAND-OFF |
RHYTEC INCORPORATED |
| K073111 |
11/05/2007 |
PORTRAIT PSR, MODEL 745915 |
RHYTEC INCORPORATED |
| K974341 |
11/18/1997 |
MITEK BTB ABSORBABLE (PLA) CROSS PIN |
MITEK PRODUCTS |
| K094017 |
12/29/2009 |
TIBIAL BASEPLATE AUGMENT MODEL KC-22118, KC-22128, KC-22138, KC-22148, KC-22158 |
OMNI LIFE SCIENCE, INC. |
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