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EXACTECH BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K896601
510(k) Type
Traditional
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1989
Days to Decision
15 days

EXACTECH BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K896601
510(k) Type
Traditional
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1989
Days to Decision
15 days