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CONELOG IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K113779
510(k) Type
Traditional
Applicant
ALTATEC GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2012
Days to Decision
358 days
Submission Type
Summary

CONELOG IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K113779
510(k) Type
Traditional
Applicant
ALTATEC GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2012
Days to Decision
358 days
Submission Type
Summary