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

QUARTEX Occipito-Cervico-Thoracic Spinal System, Globus Navigation Instruments

K Number: K211957 · Decision Aug 18, 2021
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
112
Applicant Total
51
Review Days
55

Basic Information

Device Name
QUARTEX Occipito-Cervico-Thoracic Spinal System, Globus Navigation Instruments
K Number
K211957
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Globus Medical Inc.
Date Received
June 24, 2021
Decision Date
August 18, 2021
Product Code
NKG
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
NKG Posterior Cervical Screw System

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