FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

DiversiVy™ Facet Screw System

K Number: K253432 · Decision Mar 19, 2026
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
21
Review Days
169

Basic Information

Device Name
DiversiVy™ Facet Screw System
K Number
K253432
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vy Spine, LLC
Date Received
October 1, 2025
Decision Date
March 19, 2026
Product Code
MRW
Advisory Committee
Unknown
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
MRW System, Facet Screw Spinal Device

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