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WHITESIDE ORTHOLOC MODULAR TIBIAL AUGMENTATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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