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

Equinoxe® Shoulder System

K Number: K260583 · Decision Apr 14, 2026
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
186
Review Days
53

Basic Information

Device Name
Equinoxe® Shoulder System
K Number
K260583
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Exactech, Inc.
Date Received
February 20, 2026
Decision Date
April 14, 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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Other Clearances by Exactech, Inc.

K Number Device Name
K250713 Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants
K243448 Equinoxe® Shoulder System
K243275 Equinoxe® Scapula Fracture System
K243839 Alteon® HA Femoral Stems
K240393 Exactech® TRULIANT® Knee System
K233482 Equinoxe® Central Screw Baseplate System
K230717 Exactech® Vantage® Total Ankle System
K223933 Exactech Equinoxe PHx Fracture System; Exactech EPIC Screws
K223833 Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adapter Trays
K232002 Vantage® Total Ankle System
Search all 186 clearances from Exactech, Inc. →