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

CHOICE SPINE ANTERIOR CERVICAL PLATE (ACP) SYSTEM

K Number: K091926 · Decision Dec 22, 2009
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
22
Review Days
175

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Basic Information

Device Name
CHOICE SPINE ANTERIOR CERVICAL PLATE (ACP) SYSTEM
K Number
K091926
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Choicespine, LP
Date Received
June 30, 2009
Decision Date
December 22, 2009
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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Other Clearances by Choicespine, LP

K Number Device Name
K190227 Boomerang™ Anterior Cervical Plate System
K183397 ChoiceSpine Stealth Cervical Spacer System
K182721 Choice Spine Navigation 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
Search all 22 clearances from Choicespine, LP →