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aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X NO CAM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242260
510(k) Type
Traditional
Applicant
Carlsmed, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2024
Days to Decision
107 days
Submission Type
Summary

aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X NO CAM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242260
510(k) Type
Traditional
Applicant
Carlsmed, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2024
Days to Decision
107 days
Submission Type
Summary