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FDA 510(k) Applications Submitted by ORTHOMATRIX, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010738
03/12/2001
CANNULATED PLUS SCREW SYSTEM
ORTHOMATRIX, INC.
K001254
04/19/2000
ORTHOMATRIX, INC. CERCLAGE SYSTEM
ORTHOMATRIX, INC.
K992850
08/24/1999
MAGELLAN TIBIAL INTRAMEDULLARY NAIL
ORTHOMATRIX, INC.
K992856
08/24/1999
MAGELLAN HUMERAL INTRAMEDULLARY NAIL
ORTHOMATRIX, INC.
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