FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇷 Türkiye

Mikron Spinal Fixation System

K Number: K171497 · Decision Oct 12, 2017
Classifications
1
FEI Numbers
354
Registration Numbers
354
Same Product Code
302
Applicant Total
1
Review Days
143

Basic Information

Device Name
Mikron Spinal Fixation System
K Number
K171497
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mikron Makina Sanayi Ticaret Co. Ltd.
Date Received
May 22, 2017
Decision Date
October 12, 2017
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

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