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FDA 510(k) Applications Submitted by Precifit Medical Ltd
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172568
08/25/2017
Cervage
PRECIFIT MEDICAL LTD
K173189
10/02/2017
Lumfuse TP
Precifit Medical Ltd
K163327
11/28/2016
Precifit Medical Kirschner Wires
PRECIFIT MEDICAL LTD
K171630
06/02/2017
LumFuse-TP
Precifit Medical Ltd
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