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FDA 510(k) Applications Submitted by SurgTech, Inc.,
FDA 510(k) Number
Submission Date
Device Name
Applicant
K162125
08/01/2016
MALUCÖ Total Hip Arthroplasty System
SurgTech, Inc.,
K173455
11/07/2017
SurgTech Bipolar Head System
SurgTech, Inc.,
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