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FDA 510(k) Applications Submitted by ORTHOCRAT, LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042816
10/12/2004
TRAUMACAD 1.2
ORTHOCRAT, LTD.
K073714
12/31/2007
TRAUMACAD VERSION 2.0
ORTHOCRAT, LTD.
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