FDA 510(k) Applications Submitted by JEFFREY SAKOFF

FDA 510(k) Number Submission Date Device Name Applicant
K070601 03/02/2007 MINI DRIVE-LOCK DENTAL IMPLANT SYSTEM INTRA-LOCK INTERNATIONAL
K080598 03/03/2008 MINI DRIVE-LOCK DENTAL IMPLANT SYSTEM PROSTHETICS INTRA-LOCK INTERNATIONAL
K050970 04/18/2005 MILO DENTAL IMPLANT SYSTEM INTRA-LOCK INTERNATIONAL
K021915 06/11/2002 TRANSITIONAL IMPLANTS INTRA-LOCK INTERNATIONAL
K082419 08/22/2008 REOSS POWDER, REOSS PUTTY, REOSS GEL, MODELS R-1,RP-1, RG-1 INTRA-LOCK INTERNATIONAL, INC.


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