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 |
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