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VILEX BONE PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041287
510(k) Type
Traditional
Applicant
Vilex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2004
Days to Decision
84 days
Submission Type
Statement

VILEX BONE PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041287
510(k) Type
Traditional
Applicant
Vilex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2004
Days to Decision
84 days
Submission Type
Statement