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HEMI IMPLANT; MINI HEMI IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K102401
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2011
Days to Decision
330 days
Submission Type
Summary

HEMI IMPLANT; MINI HEMI IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K102401
510(k) Type
Traditional
Applicant
VILEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2011
Days to Decision
330 days
Submission Type
Summary