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VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K991151
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1999
Days to Decision
20 days
Submission Type
Statement

VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K991151
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1999
Days to Decision
20 days
Submission Type
Statement