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WHITESIDE ORTHOLOC MODULAR TIBIAL AUGMENTATION

Page Type
Cleared 510(K)
510(k) Number
K902538
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/6/1990
Days to Decision
30 days

WHITESIDE ORTHOLOC MODULAR TIBIAL AUGMENTATION

Page Type
Cleared 510(K)
510(k) Number
K902538
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/6/1990
Days to Decision
30 days