FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

Blue Mountain Cervical Plate System

K Number: K150036 · Decision May 7, 2015
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
5
Review Days
118

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Basic Information

Device Name
Blue Mountain Cervical Plate System
K Number
K150036
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spineway
Date Received
January 9, 2015
Decision Date
May 7, 2015
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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Other Clearances by Spineway

K Number Device Name
K231658 VEOS Spinal Fixation System
K162694 Ayers Rock Cervical interbody fusion system
K152355 Twin Peaks Lumbar Interbody Fusion System
K150185 Mont Blanc Spinal System