Last synced on 14 November 2025 at 11:06 pm

COLUMBUS REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K083772
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2009
Days to Decision
168 days
Submission Type
Summary

COLUMBUS REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K083772
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2009
Days to Decision
168 days
Submission Type
Summary