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

Ventana™ A Anterior Lumbar Interbody System

K Number: K253559 · Decision Feb 25, 2026
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
49
Review Days
100

Basic Information

Device Name
Ventana™ A Anterior Lumbar Interbody System
K Number
K253559
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal Elements, Inc.
Date Received
November 17, 2025
Decision Date
February 25, 2026
Product Code
OVD
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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