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FDA 510(k) Applications Submitted by U & I CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180759
03/22/2018
SECULOKÖ Suture Anchor
U & I Corporation
K131200
04/29/2013
ASPIRON ACP SYSTEM
U & I CORPORATION
K132797
09/06/2013
L'DISQ
U & I CORPORATION
K183383
12/06/2018
ANAXÖ OCT Spinal System
U & I Corporation
K132101
07/08/2013
ANAX 5.5 SPINAL SYSTEM
U & I CORPORATION
K132218
07/17/2013
PERFIX ILIAC SCREW SYSTEM
U & I CORPORATION
K143631
12/22/2014
Benefix Interspinous Fixation System
U & I Corporation
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