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

STRUXXURE®-L and STRUXXURE®-A Plate System

K Number: K202192 · Decision Sep 17, 2020
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
14
Review Days
43

Basic Information

Device Name
STRUXXURE®-L and STRUXXURE®-A Plate System
K Number
K202192
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nexxt Spine LLC
Date Received
August 5, 2020
Decision Date
September 17, 2020
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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