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VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014154
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2002
Days to Decision
90 days
Submission Type
Statement

VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014154
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2002
Days to Decision
90 days
Submission Type
Statement