FDA 510(k) Applications Submitted by Julie Vafides

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130105	01/15/2013	RIGIDFIX CURVE ST ACL PLA CROSS PIN SYSTEM, RIGIDFIX CURVE ST ACL PEEK CROSS PIN SYSTEM	DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K130539	03/01/2013	HEALIX ADVANCE KNOTLESS PEEK ANCHOR (4.75MM)(5.5MM)	DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K170639	03/02/2017	HEALIX ADVANCE Anchor with PERMATAPE Suture	Medos International SARL
K171114	04/14/2017	HEALIX ADVANCE KNOTLESS Anchor	Medos International SARL
K141259	05/15/2014	GRYPHON BR ANCHOR WITH PERMACORD, GRYPHON BR DS ANCHOR WITH PERMACORD,GRYPHON PEEK ANCHOR WITH PERMACORD, GRYPHON PEEK	DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K122123	07/18/2012	6-8MM X 30 MM INTRAFIX PEEK TAPERED SCREW 7-9MM X 30MM INTRAFIX PEEK TAPERED SCREW 8-10MM X 30 MM INTRAFIX PEEK TAPERED	DEPUY MITEK INC., A JOHNSON AND JOHNSON COMPANY