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

Exceed® Biplanar Expandable Interbody System

K Number: K261159 · Decision May 29, 2026
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
59
Review Days
51

Basic Information

Device Name
Exceed® Biplanar Expandable Interbody System
K Number
K261159
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spine Wave, Inc.
Date Received
April 8, 2026
Decision Date
May 29, 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

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