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ACRON™ TLIF System

Page Type
Cleared 510(K)
510(k) Number
K171151
510(k) Type
Traditional
Applicant
SpineMED Ges.m.b.H
Country
Austria
FDA Decision
Substantially Equivalent
Decision Date
4/27/2018
Days to Decision
372 days
Submission Type
Summary

ACRON™ TLIF System

Page Type
Cleared 510(K)
510(k) Number
K171151
510(k) Type
Traditional
Applicant
SpineMED Ges.m.b.H
Country
Austria
FDA Decision
Substantially Equivalent
Decision Date
4/27/2018
Days to Decision
372 days
Submission Type
Summary