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FDA 510(k) Applications Submitted by BTLOCK SRL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K073458
12/10/2007
BT-TITE ONE(BTICV1), BT-TITE STANDARD(BTIVSM), BT-TITE CV2(BTICV2)
BTLOCK SRL
K083869
12/29/2008
BT-TITE CV3, MINI IMPLANT, MINI SINGLE, SLOT IMPLANT, MODEL(S) DDDIII BTICV3, 1, AND DDDIIIBTISI
BTLOCK SRL
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