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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