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

ChoiceSpine Stealth Cervical Spacer System

K Number: K183397 · Decision Mar 6, 2019
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
22
Review Days
89

Basic Information

Device Name
ChoiceSpine Stealth Cervical Spacer System
K Number
K183397
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Choicespine, LP
Date Received
December 7, 2018
Decision Date
March 6, 2019
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

Similar 510(k) Clearances

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

View all

Other Clearances by Choicespine, LP

K Number Device Name
K190227 Boomerang™ Anterior Cervical Plate 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
K170953 Tomcat Cervical Spinal System
Search all 22 clearances from Choicespine, LP →