FDA 510(k) Applications Submitted by Brian Young
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K030311 |
01/30/2003 |
HEM-O-LOK XL CLIP |
WECK |
K170411 |
02/10/2017 |
ER-REBOA Catheter |
Prytime Medical Devices, Inc |
K200459 |
02/25/2020 |
pREBOA-PRO Catheter |
Prytime Medical Devices, Inc. |
K011660 |
05/29/2001 |
WECK CARDIAC PACING WIRES |
WECK CLOSURE SYSTEMS |
K982313 |
07/01/1998 |
HORIZON TITANIUM CLIPS, HORIZON TANTALUM CLIPS |
WECK CLOSURE SYSTEMS |
K061939 |
07/10/2006 |
MODIFICATION TO ALLOMATRIX CUSTOM |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K172790 |
09/15/2017 |
ER-REBOA Catheter |
Prytime Medical Devices, Inc. |
K993157 |
09/21/1999 |
HEM-O-LOK SMX POLYMER CLIPS, MODEL 544220, HEM-0-LOK MLX POLYMER CLIPS, MODEL 544240 |
WECK CLOSURE SYSTEMS |
K133232 |
10/21/2013 |
PREVENA INCISION MANAGEMENT SYSTEM WITH CUSTOMIZABLE DRESSING, PREVENA INCISION MANAGEMANT SYSTEM WITH PEEL& PLACE DRES |
KCI USA, INC. (KINETIC CONCEPTS, INC.) |
K003337 |
10/25/2000 |
HEM-O-LOK SMX, MODEL 544220; HEM-O-LOK ML, MODEL 544230; HEM-O-LOK MLX, MODEL 544240 |
WECK CLOSURE SYSTEMS |
K053319 |
11/30/2005 |
ALLOMATRIX CUSTOM |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K193440 |
12/11/2019 |
ER-REBOA PLUS Catheter |
Prytime Medical Devices, Inc |
K060011 |
01/03/2006 |
MIIG SR |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K041663 |
06/18/2004 |
ALLOMATRIX TCP, ALLOMATRIX W/CASO4 FILLED TCP, AND ALLOMATRIX PLUS CBM |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K982944 |
08/21/1998 |
HEM-O-LOCK, MODEL 523935 |
WECK CLOSURE SYSTEMS |
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