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

NuVasive Pulse System

K Number: K210574 · Decision Jul 29, 2021
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
112
Review Days
153

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Basic Information

Device Name
NuVasive Pulse System
K Number
K210574
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nu Vasive, Incorporated
Date Received
February 26, 2021
Decision Date
July 29, 2021
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OLO), ordered by most recent decision date.

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Other Clearances by Nu Vasive, Incorporated

K Number Device Name
K231735 NuVasive CoRoent Small Interbody System; NuVasive CoRoent Small Contoured Interbody System; NuVasive CoRoent Small Interlock System; NuVasive CoRoent Small Interlock II System; NuVasive CoRoent Small Ti-C System; NuVasive Cohere Cervical Interbody System
K230894 NuVasive Modulus ALIF System
K230989 Rod Registration Frame
K223181 NuVasive Reline System
K221751 NuVasive Cohere ALIF System Intervertebral Body Fusion Device
K221388 NuVasive Reline Cervical System
K220478 NuVasive MOD-EX XLIF Interbody System, NuVasive MOD-EX XLIF Plated 2.0 Interbody System
K213654 NuVasive Reline Cervical System
K203714 NuVasive Thoracolumbar Interbody Systems: NuVasive CoRoent Thoracolumbar System, NuVasive CoRoent XL Interfixated System, Brigade System, Brigade Lateral System, BASE Interfixated Titanium System, Coalesce Thoracolumbar Interbody Fusion System, NuVasive Cohere Thoracolumbar Interbody System, NuVasive Modulus XLIF Interbody System, NuVasive Modulus TLIF Interbody System, NuVasive Modulus ALIF System, NuVasive Attrax Putty
K212446 NuVasive Anterior Cervical Plate Systems
Search all 112 clearances from Nu Vasive, Incorporated →