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

Choice Spine Navigation System

K Number: K182721 · Decision Jan 8, 2019
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
22
Review Days
102

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Basic Information

Device Name
Choice Spine Navigation System
K Number
K182721
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Choicespine, LP
Date Received
September 28, 2018
Decision Date
January 8, 2019
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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Other Clearances by Choicespine, LP

K Number Device Name
K190227 Boomerang™ Anterior Cervical Plate System
K183397 ChoiceSpine Stealth Cervical Spacer System
K183214 Raven Lumbar Plate System
K180519 HARRIER-SA™ Lumbar Interbody System
K172816 TiGer Shark™ System
K173215 Choice Spine Laminoplasty™ Fixation System
K171489 Acapella Cervical Spacer System
K170821 ChoiceSpine™ Proliant® Posterior Pedicle Screw and Hook Fixation System
K170942 The Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems
K170953 Tomcat Cervical Spinal System
Search all 22 clearances from Choicespine, LP →