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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