FDA 510(k) Applications Submitted by ROGER D BROWN

FDA 510(k) Number Submission Date Device Name Applicant
K020895 03/19/2002 ALLOMATRIX MODEL# 86 WRIGHT MEDICAL TECHNOLOGY, INC.
K040980 04/15/2004 ALLOMATRIX C PUTTY, ALLOMATRIX CUSTOM PUTTY, ALLOMATRIX DR PUTTY, IGNITE SCAFFOLD, MODELS 860C, 86XC, 86DR, 860D, 860T WRIGHT MEDICAL TECHNOLOGY, INC.
K021346 04/29/2002 STEM HIP REPLACEMENT SYSTEM, MODEL PHA002XX WRIGHT MEDICAL TECHNOLOGY, INC.
K041168 05/04/2004 ALLOMATRIX PUTTY WRIGHT MEDICAL TECHNOLOGY, INC.
K971946 05/27/1997 NPB-190 PULSE OXIMETER (NPB-190) NELLCOR PURITAN BENNETT, INC.
K972468 07/01/1997 NPB-195 PULSE OXIMETER NELLCOR PURITAN BENNETT, INC.
K972837 07/31/1997 NPB-290 PULSE OXIMETER (NPB-290) NELLCOR PURITAN BENNETT, INC.
K973147 08/22/1997 NPB-295 PULSE OXIMETER NELLCOR PURITAN BENNETT, INC.
K022828 08/26/2002 OSTEOSET DBM PELLETS, MODEL 8600-48XX WRIGHT MEDICAL TECHNOLOGY, INC.
K023088 09/17/2002 BONE GRAFT SYRINGE, MODEL 8600-00X0 WRIGHT MEDICAL TECHNOLOGY, INC.


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