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

Arthrex Distal Radius System

K Number: K143749 · Decision Apr 3, 2015
Classifications
1
FEI Numbers
505
Registration Numbers
505
Same Product Code
1254
Applicant Total
36
Review Days
93

Basic Information

Device Name
Arthrex Distal Radius System
K Number
K143749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
December 31, 2014
Decision Date
April 3, 2015
Product Code
HRS
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
HRS Plate, Fixation, Bone

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