Last synced on 14 November 2025 at 11:06 pm

aprevo® posterior/transforaminal lumbar interbody fusion device

Page Type
Cleared 510(K)
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)
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