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WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP

Page Type
Cleared 510(K)
510(k) Number
K915525
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1993
Days to Decision
512 days
Submission Type
Statement

WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP

Page Type
Cleared 510(K)
510(k) Number
K915525
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1993
Days to Decision
512 days
Submission Type
Statement