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DEPUY CANNULATED BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K893512
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1989
Days to Decision
108 days

DEPUY CANNULATED BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K893512
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1989
Days to Decision
108 days