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ADVANCE MODULAR TIBIAL COMPONENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973524
510(k) Type
Traditional
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/12/1997
Days to Decision
86 days

ADVANCE MODULAR TIBIAL COMPONENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973524
510(k) Type
Traditional
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/12/1997
Days to Decision
86 days