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VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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