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

Exactech Equinoxe Stemless Shoulder

K Number: K173388 · Decision Mar 9, 2018
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
18
Applicant Total
186
Review Days
130

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Basic Information

Device Name
Exactech Equinoxe Stemless Shoulder
K Number
K173388
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
October 30, 2017
Decision Date
March 9, 2018
Product Code
PKC
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
PKC Prosthesis, Total Anatomic Shoulder, Uncemented Metaphyseal Humeral Stem With No Diaphyseal Incursion, Semi-Constrained

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PKC), ordered by most recent decision date.

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Other Clearances by Exactech, Inc.

K Number Device Name
K260583 Equinoxe® Shoulder System
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
Search all 186 clearances from Exactech, Inc. →