Last synced on 25 January 2026 at 3:41 am

aprevo® Anterior and Lateral Lumbar Interbody Fusion device (ALIF/LLIF); aprevo® Transforaminal Lumbar Interbody Fusion device (TLIF); aprevo® Anterior Lumbar Interbody Fusion device with Interfixation (ALIF-X)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241328
510(k) Type
Traditional
Applicant
Carlsmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2024
Days to Decision
94 days
Submission Type
Summary

aprevo® Anterior and Lateral Lumbar Interbody Fusion device (ALIF/LLIF); aprevo® Transforaminal Lumbar Interbody Fusion device (TLIF); aprevo® Anterior Lumbar Interbody Fusion device with Interfixation (ALIF-X)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241328
510(k) Type
Traditional
Applicant
Carlsmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2024
Days to Decision
94 days
Submission Type
Summary