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

Acapella Cervical Spacer System

K Number: K171489 · Decision Oct 23, 2017
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
22
Review Days
154

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Basic Information

Device Name
Acapella Cervical Spacer System
K Number
K171489
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Choicespine, LP
Date Received
May 22, 2017
Decision Date
October 23, 2017
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Similar 510(k) Clearances

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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
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 →