Carlsmed, Inc.
FDA 510(k) medical device clearances.
Top product codes for Carlsmed, Inc.
Recent clearances by Carlsmed, Inc.
- K252894 — aprevo® cervical interbody system
- K252611 — aprevo® cervical plating system
- K250827 — 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
- K250987 — aprevo® posterior/transforaminal lumbar interbody fusion device
- K243802 — aprevo® anterior and lateral lumbar interbody fusion device, aprevo® anterior lumbar interbody fusion device with interfixation
- K242599 — aprevo® Digital Planning
- K243635 — aprevo® anterior lumbar interbody fusion device with interfixation
- K242260 — aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X NO CAM
- K241477 — aprevo® anterior lumbar interbody fusion device with interfixation
- K241332 — aprevo® anterior and lateral lumbar interbody fusion device; aprevo® anterior lumbar interbody fusion devices with interfixation; aprevo® transforaminal lumbar interbody fusion device
- K241328 — 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)
- K232282 — aprevo® anterior and lateral lumbar interbody fusion device, aprevo® transforaminal lumbar interbody fusion device
- K231955 — aprevo® Digital Segmentation
- K231140 — aprevo® transforaminal lumbar interbody fusion device
- K222195 — aprevo® Digital Workflow
- K222009 — aprevo® anterior lumbar interbody fusion device with interfixation
- K222082 — aprevo® anterior and lateral lumbar interbody fusion devices, aprevo® transforaminal lumbar interbody fusion devices
- K210542 — aprevo Transforaminal IBF
- K202034 — aprevo Intervertebral Body Fusion Device
Data sourced from openFDA. This site is unofficial and independent of the FDA.