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CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023684
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2004
Days to Decision
486 days
Submission Type
Statement

CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023684
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2004
Days to Decision
486 days
Submission Type
Statement