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

BLACKBIRD SPINAL SYSTEM

K Number: K133214 · Decision Mar 7, 2014
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
22
Review Days
140

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Basic Information

Device Name
BLACKBIRD SPINAL SYSTEM
K Number
K133214
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Choicespine, LP
Date Received
October 18, 2013
Decision Date
March 7, 2014
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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K Number Device Name
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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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