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COORDINATE REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K955884
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1996
Days to Decision
76 days
Submission Type
Summary

COORDINATE REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K955884
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1996
Days to Decision
76 days
Submission Type
Summary