FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Anatomical Shoulder System

K Number: K193099 · Decision Jan 29, 2020
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
43
Review Days
83

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Basic Information

Device Name
Anatomical Shoulder System
K Number
K193099
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer GmbH
Date Received
November 7, 2019
Decision Date
January 29, 2020
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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