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VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K973309
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/16/1998
Days to Decision
135 days

VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K973309
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/16/1998
Days to Decision
135 days