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Align Cervical Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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