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

Integra TITAN Reverse Shoulder System

K Number: K173717 · Decision Jun 21, 2018
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
182
Applicant Total
13
Review Days
198

Basic Information

Device Name
Integra TITAN Reverse Shoulder System
K Number
K173717
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Integra LifeSciences Corporation
Date Received
December 5, 2017
Decision Date
June 21, 2018
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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