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FDA 510(k) Applications Submitted by ARC SURGICAL LLC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K141559
06/12/2014
V-GUIDE FOR VENTRICULOSTOMIES
ARC SURGICAL LLC.
K071616
06/13/2007
ARC SURGICAL BIOTRAK PIN SYSTEM
ARC SURGICAL LLC.
K061763
06/22/2006
ARC SURGICAL BIOTRAK SCREW
ARC SURGICAL LLC.
K063244
10/26/2006
ARC SURGICAL BONE REDUCTION SCREW
ARC SURGICAL LLC.
K043176
11/16/2004
ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM
ARC SURGICAL LLC.
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