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

HARRIER-SA™ Lumbar Interbody System

K Number: K180519 · Decision May 16, 2018
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
22
Review Days
78

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Basic Information

Device Name
HARRIER-SA™ Lumbar Interbody System
K Number
K180519
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
February 27, 2018
Decision Date
May 16, 2018
Product Code
OVD
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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K171489 Acapella Cervical Spacer System
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K170942 The Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems
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