FDA 510(k) Applications Submitted by BIOPRO, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K130298 |
02/07/2013 |
BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM |
BIOPRO, INC. |
K121973 |
07/05/2012 |
BIOPRO HEMI-EDGE TOE SYSTEM |
BIOPRO, INC. |
K132510 |
08/12/2013 |
BIOPRO - INFINITY PLATE ANCHOR SYSTEM |
BIOPRO, INC. |
K162674 |
09/26/2016 |
BioPro Foot Plating Systems |
BIOPRO, INC. |
K010149 |
01/17/2001 |
WUJIN #3 FEMORAL NAIL |
BIOPRO, INC. |
K990821 |
03/11/1999 |
PROVIDENCE CUP SYSTEM |
BIOPRO, INC. |
K001046 |
03/31/2000 |
BIOPRO GLENOID COMPONENT W/ KEEL & W/ POSTS |
BIOPRO, INC. |
K163627 |
12/22/2016 |
Shotel Ankle Arthrodesis Nail System |
BioPro, Inc. |
K041595 |
06/14/2004 |
TOE MP JOINT, MODELS 10412-10414, 14958, 14960, 1060-10062,16818,-16822,16867-16870 |
BIOPRO, INC. |
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. |
K960467 |
01/30/1996 |
POWDER FREE LATEX EXAMINATION GLOVE |
BIOPRO, INC. |
K011459 |
05/11/2001 |
WUJIN #3 FEMORAL BONE PLATE |
BIOPRO, INC. |
K011460 |
05/11/2001 |
WUJIN #3 TIBIAL BONE PLATE |
BIOPRO, INC. |
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