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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