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WHITESIDE ORTHOLOC MOD.TIBIAL AUGMENTATION COMP

Page Type
Cleared 510(K)
510(k) Number
K914169
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1992
Days to Decision
132 days
Submission Type
Statement

WHITESIDE ORTHOLOC MOD.TIBIAL AUGMENTATION COMP

Page Type
Cleared 510(K)
510(k) Number
K914169
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1992
Days to Decision
132 days
Submission Type
Statement