FDA 510(k) Applications Submitted by DAVID MRAK
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090208 |
01/28/2009 |
BIOPRO FEMORAL HEADS |
BIOPRO, INC. |
| K100761 |
03/17/2010 |
BIOPRO POLAR HEAD |
BIOPRO, INC. |
| K101030 |
04/13/2010 |
MODIFICATION TO HBS HEADLESS BONE SCREW |
BIOPRO, INC. |
| K061089 |
04/18/2006 |
MODULAR THUMB IMPLANT, MODELS 17600, 17601, 17602, 17603, 17596, 17597, 17598, 17599 |
BIOPRO, INC. |
| K081149 |
04/22/2008 |
BIOPRO GO-EZ SCREW |
BIOPRO, INC. |
| K061798 |
06/26/2006 |
BIOPRO MEMORY STAPLE |
BIOPRO, INC. |
| K041936 |
07/19/2004 |
BIOPRO SUBTALAR IMPLANT |
BIOPRO, INC. |
| K072298 |
08/17/2007 |
BIOPRO MEMORY STAPLE, MODELS 18062-18073 |
BIOPRO, INC. |
| K082705 |
09/16/2008 |
BIOPRO BIPOLAR HEAD, MODELS 18130-18152 |
BIOPRO, INC. |
| K052596 |
09/21/2005 |
MODULAR THUMB IMPLANT, MODELS 17065,17066,17243,17067,17199,17238,17005,17239,17006,17240,17007,17241,17500,17501,17507 |
BIOPRO, INC. |
| K083490 |
11/25/2008 |
BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685 |
BIOPRO, INC. |
| K043542 |
12/23/2004 |
BIOPRO TARA FEMORAL RESURFACING COMPONENT |
BIOPRO, INC. |
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