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FDA 510(k) Applications Submitted by KRISTI FRISCH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130640
03/11/2013
ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM
MEDTRONIC SOFAMOR DANEK USA, INC.
K231113
04/19/2023
Arthrex FiberTak Suture Anchor
Arthrex Inc.
K141632
06/18/2014
ZEVO (TM) ANTERIOR CERVICAL PLATE SYSTEM
MEDTRONIC SOFAMOR DANEK USA, INC.
K231857
06/23/2023
Arthrex TightRope II
Arthrex Inc.
K113252
11/03/2011
PEEK PREVAIL CERVICAL INTERBODY DEVICE
MEDTRONIC SOFAMOR DANEK
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