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ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K932210
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
9/7/1994
Days to Decision
488 days
Submission Type
Summary

ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K932210
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
9/7/1994
Days to Decision
488 days
Submission Type
Summary