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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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