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

Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System

K Number: K253748 · Decision Jan 23, 2026
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
84
Review Days
59

Basic Information

Device Name
Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System
K Number
K253748
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Life Spine, Inc.
Date Received
November 25, 2025
Decision Date
January 23, 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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