Last synced on 25 January 2026 at 3:41 am

aprevo® anterior lumbar interbody fusion device; aprevo® lateral lumbar interbody fusion device; aprevo® anterior lumbar interbody fusion device with interfixation; aprevo® transforaminal lumbar interbody fusion device; aprevo® TLIF-CA Articulating System; aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X No Cams

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250827
510(k) Type
Traditional
Applicant
Carlsmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2025
Days to Decision
111 days
Submission Type
Summary

aprevo® anterior lumbar interbody fusion device; aprevo® lateral lumbar interbody fusion device; aprevo® anterior lumbar interbody fusion device with interfixation; aprevo® transforaminal lumbar interbody fusion device; aprevo® TLIF-CA Articulating System; aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X No Cams

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250827
510(k) Type
Traditional
Applicant
Carlsmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2025
Days to Decision
111 days
Submission Type
Summary