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ArtFX Spinal Fixation System

Page Type
Cleared 510(K)
510(k) Number
K212220
510(k) Type
Traditional
Applicant
ArtFX Medical LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2023
Days to Decision
643 days
Submission Type
Summary

ArtFX Spinal Fixation System

Page Type
Cleared 510(K)
510(k) Number
K212220
510(k) Type
Traditional
Applicant
ArtFX Medical LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2023
Days to Decision
643 days
Submission Type
Summary