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COLUMBUS TOTAL KNEE SYSTEM AS COLUMBUS REVISION KNEE SYSTEM ENDURO KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120955
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2012
Days to Decision
262 days
Submission Type
Summary

COLUMBUS TOTAL KNEE SYSTEM AS COLUMBUS REVISION KNEE SYSTEM ENDURO KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120955
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2012
Days to Decision
262 days
Submission Type
Summary