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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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