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

MySpine Pedicle Screw Placement Guides – MC and Drill Pilot Instruments

K Number: K173472 · Decision Apr 19, 2018
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
7
Applicant Total
165
Review Days
161

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Basic Information

Device Name
MySpine Pedicle Screw Placement Guides – MC and Drill Pilot Instruments
K Number
K173472
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medacta International S.A.
Date Received
November 9, 2017
Decision Date
April 19, 2018
Product Code
PQC
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
PQC Pedicle Screw Placement Guide

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Other Clearances by Medacta International S.A.

K Number Device Name
K254202 MectaLIF 3D Metal Anterior
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K250644 MSS - Monobloc stem
K251043 Mpact 3D Metal Implants Extension – DMLS Technology
K252847 NextAR Hip Platform
K242603 MyPAO SA guides
K250338 MSS - Humeral reverse liners extension
K250450 Coated hip implants
K252225 PowerKnot High Strength Sutures
Search all 165 clearances from Medacta International S.A. →