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ARTFX Trauma Bone Plate and Screw System

Page Type
Cleared 510(K)
510(k) Number
K242939
510(k) Type
Traditional
Applicant
ARTFX Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2024
Days to Decision
89 days
Submission Type
Summary

ARTFX Trauma Bone Plate and Screw System

Page Type
Cleared 510(K)
510(k) Number
K242939
510(k) Type
Traditional
Applicant
ARTFX Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2024
Days to Decision
89 days
Submission Type
Summary