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ADVANCE 913 MEDIAL PIVOT TIBIAL INSERT, ADVANCE 913 MEDIAL PIVOT TIBIAL BASE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092201
510(k) Type
Special
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2009
Days to Decision
29 days
Submission Type
Summary

ADVANCE 913 MEDIAL PIVOT TIBIAL INSERT, ADVANCE 913 MEDIAL PIVOT TIBIAL BASE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092201
510(k) Type
Special
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2009
Days to Decision
29 days
Submission Type
Summary