Last synced on 25 January 2026 at 3:41 am

aprevo® posterior/transforaminal lumbar interbody fusion device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250987
510(k) Type
Traditional
Applicant
Carlsmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2025
Days to Decision
91 days
Submission Type
Summary

aprevo® posterior/transforaminal lumbar interbody fusion device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250987
510(k) Type
Traditional
Applicant
Carlsmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2025
Days to Decision
91 days
Submission Type
Summary