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Acro Composites Interbody System

Page Type
Cleared 510(K)
510(k) Number
K230478
510(k) Type
Traditional
Applicant
Acro Composites, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2023
Days to Decision
239 days
Submission Type
Summary

Acro Composites Interbody System

Page Type
Cleared 510(K)
510(k) Number
K230478
510(k) Type
Traditional
Applicant
Acro Composites, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2023
Days to Decision
239 days
Submission Type
Summary