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Align Cervical Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K230639
510(k) Type
Traditional
Applicant
Acuity Surgical Devices, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2023
Days to Decision
268 days
Submission Type
Summary

Align Cervical Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K230639
510(k) Type
Traditional
Applicant
Acuity Surgical Devices, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2023
Days to Decision
268 days
Submission Type
Summary