FDA 510(k) Applications Submitted by Depuy Mitek, a Johnson and Johnson Company

FDA 510(k) Number	Submission Date	Device Name	Applicant
K150209	01/30/2015	Healix BR Anchor, Healix PEEK Anchor, Healix Transtend, Gryphon T and P BR Anchor, Gryphon PEEK Anchor, VersaLok Anchor, Bioknotless BR Anchor, Lupine BR Anchor, PanaLok Anchor,PanaLok Anchor with Orthocord, PanaLok RC QuickAnchor Plus; PanaLok RC QuickAn	Depuy Mitek, a Johnson and Johnson Company
K140324	02/10/2014	RIGIDLOOP ADJUSTABLE CORTICAL IMPLANT: STANDARD, LONG AND XL	DEPUY MITEK, A JOHNSON AND JOHNSON COMPANY
K140643	03/12/2014	GRYPHON BR ANCHOR W/PROKNOT TECHNOLOGY,GRYPHON PEEK ANCHOR W/ PROKNOT TECHNOLOGY	DEPUY MITEK, A JOHNSON AND JOHNSON COMPANY