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