FDA 510(k) Applications Submitted by Carlsmed, Inc

FDA 510(k) Number Submission Date Device Name Applicant
K241328 05/10/2024 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) Carlsmed, Inc
K242260 07/31/2024 aprevo« Cervical ACDF; aprevo« Cervical ACDF-X; aprevo« Cervical ACDF-X NO CAM Carlsmed, Inc


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact