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PROSTEHSIS, TOTAL KNEE REPLACEMENT

Page Type
Cleared 510(K)
510(k) Number
K760334
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1976
Days to Decision
13 days

PROSTEHSIS, TOTAL KNEE REPLACEMENT

Page Type
Cleared 510(K)
510(k) Number
K760334
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1976
Days to Decision
13 days