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

DuraPro™ Oscillating System

K Number: K240568 · Decision Apr 29, 2024
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
404
Applicant Total
11
Review Days
60

Basic Information

Device Name
DuraPro™ Oscillating System
K Number
K240568
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Globus Medical, Inc.
Date Received
February 29, 2024
Decision Date
April 29, 2024
Product Code
OLO
Advisory Committee
Neurology
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
OLO Orthopedic Stereotaxic Instrument

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