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COLUMBUS REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122985
510(k) Type
Special
Applicant
AESCULAP IMPLANT SYSTEM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2012
Days to Decision
30 days
Submission Type
Summary

COLUMBUS REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122985
510(k) Type
Special
Applicant
AESCULAP IMPLANT SYSTEM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2012
Days to Decision
30 days
Submission Type
Summary