Last synced on 25 January 2026 at 3:41 am

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

Page Type
Cleared 510(K)
PDF
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
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