Last synced on 30 May 2025 at 11:05 pm

VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX, S30-XX, P235-XX, S35-XX, P240-XX, S40-XX, P24

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991197
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1999
Days to Decision
19 days
Submission Type
Statement

VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX, S30-XX, P235-XX, S35-XX, P240-XX, S40-XX, P24

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991197
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1999
Days to Decision
19 days
Submission Type
Statement