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EXTREMITY BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K963118
510(k) Type
Traditional
Applicant
ACUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/10/1996
Days to Decision
59 days

EXTREMITY BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K963118
510(k) Type
Traditional
Applicant
ACUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/10/1996
Days to Decision
59 days