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

Veritas Reverse Total Shoulder System

K Number: K253992 · Decision May 7, 2026
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
12
Review Days
146

Basic Information

Device Name
Veritas Reverse Total Shoulder System
K Number
K253992
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Restor3D
Date Received
December 12, 2025
Decision Date
May 7, 2026
Product Code
PHX
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
PHX Shoulder Prosthesis, Reverse Configuration

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