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

Orthofix MJ-FLEX THE NEW METAIZEAU NAIL

K Number: K173051 · Decision Nov 16, 2017
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
38
Review Days
49

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Basic Information

Device Name
Orthofix MJ-FLEX THE NEW METAIZEAU NAIL
K Number
K173051
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthofix Srl
Date Received
September 28, 2017
Decision Date
November 16, 2017
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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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 →