FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra™ cervical plating system

K Number: K260385 · Decision May 9, 2026
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
21
Review Days
92

Basic Information

Device Name
aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra™ cervical plating system
K Number
K260385
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carlsmed, Inc.
Date Received
February 6, 2026
Decision Date
May 9, 2026
Product Code
MAX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MAX), ordered by most recent decision date.

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Other Clearances by Carlsmed, Inc.

K Number Device Name
K260570 corra™ cervical plating system
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
Search all 21 clearances from Carlsmed, Inc. →