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

Atlas Spine Project X Expandable Posterior Lumbar Interbody System

K Number: K251969 · Decision Aug 15, 2025
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
15
Review Days
50

Basic Information

Device Name
Atlas Spine Project X Expandable Posterior Lumbar Interbody System
K Number
K251969
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Atlas Spine, Inc.
Date Received
June 26, 2025
Decision Date
August 15, 2025
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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