FDA 510(k) Applications Submitted by ALTATEC BIOTECHNOLOGIES

FDA 510(k) Number Submission Date Device Name Applicant
K000065 01/10/2000 CAMLOG CYLINDER IMPLANT SYSTEM ALTATEC BIOTECHNOLOGIES
K000099 01/13/2000 CAMLOG SCREW IMPLANT SYSTEM ALTATEC BIOTECHNOLOGIES
K000100 01/13/2000 CAMLOG ROOTFORM IMPLANT SYSTEM ALTATEC BIOTECHNOLOGIES
K032448 08/08/2003 ALTATEC CERAMIC ABUTMENT ALTATEC BIOTECHNOLOGIES


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