FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

OrthoNext Platform System

K Number: K202519 · Decision Oct 27, 2020
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
38
Review Days
56

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Basic Information

Device Name
OrthoNext Platform System
K Number
K202519
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthofix Srl
Date Received
September 1, 2020
Decision Date
October 27, 2020
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

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Other Clearances by Orthofix Srl

K Number Device Name
K260146 FITBONE® TRANSPORT AND LENGTHENING SYSTEM
K253991 Fitbone™ Trochanteric, FITBONE® Transport and Lengthening System, FITBONE® TAA
K250112 FitboneTM Trochanteric
K242270 OrthoNext Platform System
K242861 TrueLok Elevate
K233867 Fitbone Trochanteric
K232648 RODEO Telescopic Nail
K232169 FITBONE® Transport and Lengthening System
K213572 JuniOrtho Plating System™
K212044 TrueLok Evo
Search all 38 clearances from Orthofix Srl →