FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

INHANCE™ Reverse Shoulder System

K Number: K253624 · Decision Mar 11, 2026
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
48
Review Days
113

Basic Information

Device Name
INHANCE™ Reverse Shoulder System
K Number
K253624
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy Ireland UC
Date Received
November 18, 2025
Decision Date
March 11, 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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