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

CHOICE SPINE LUMBAR SPACER SYSTEM (SABRE, SHARK, HORNET, HARPOON)

K Number: K140142 · Decision Jul 16, 2014
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
22
Review Days
175

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Basic Information

Device Name
CHOICE SPINE LUMBAR SPACER SYSTEM (SABRE, SHARK, HORNET, HARPOON)
K Number
K140142
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
January 22, 2014
Decision Date
July 16, 2014
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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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
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