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

NEXXT MATRIXX Stand Alone ALIF System

K Number: K202230 · Decision Dec 15, 2020
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
22
Review Days
130

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Basic Information

Device Name
NEXXT MATRIXX Stand Alone ALIF System
K Number
K202230
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nexxt Spine, LLC
Date Received
August 7, 2020
Decision Date
December 15, 2020
Product Code
OVD
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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