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FDA 510(k) Applications Submitted by ANGELA MALLERY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040119
01/20/2004
PERI-STRIPS STAPLE LINE REINFORCEMENT-SLEEVE CONFIGURATION, PERI-STRIPS STAPLE LINE REINFORCEMENT-STRIP CONFIGURATION
SYNOVIS SURGICAL INNOVATIONS
K040415
02/18/2004
PERI-STRIPS STAPLE LINE REINFORCEMENT - SLEEVE AND STRIP CONFIGURATIONS - AND PERI-STRIPS DRY STAPLE LINE REINFORCEMENT
SYNOVIS SURGICAL INNOVATIONS
K220759
03/15/2022
Armis VeriCyn Wound Wash
Armis Biopharma, Inc.
K230743
03/16/2023
ICHOR 14F Embolectomy System
ICHOR
K030879
03/20/2003
VERITAS COLLAGEN MATRIX
SYNOVIS SURGICAL INNOVATIONS
K991194
04/08/1999
MODIFICATION TO ULTRA-SELECT GUIDEWIRE
MICROVENA CORP.
K191275
05/13/2019
AllÆInCath 035M PTA Balloon Dilatation Catheter
NexStep Medical
K991898
06/04/1999
ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE
MICROVENA CORP.
K201631
06/16/2020
VersaWrap Nerve Protector
Alafair Biosciences Inc
K213163
09/28/2021
VersaWrap
Alafair Biosciences Inc
K213173
09/28/2021
TrabEx Pro
MicroSurgical Technologies Inc
K203600
12/09/2020
VersaWrap
Alafair Biosciences Inc
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