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JONES-FX FRACTURE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131620
510(k) Type
Traditional
Applicant
INSTRATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2013
Days to Decision
52 days
Submission Type
Summary

JONES-FX FRACTURE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131620
510(k) Type
Traditional
Applicant
INSTRATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2013
Days to Decision
52 days
Submission Type
Summary