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

Belvedere™ Lateral Plating System

K Number: K153097 · Decision Jul 15, 2016
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
15
Review Days
263

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Basic Information

Device Name
Belvedere™ Lateral Plating System
K Number
K153097
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neurostructures, Inc.
Date Received
October 26, 2015
Decision Date
July 15, 2016
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

Similar 510(k) Clearances

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Other Clearances by Neurostructures, Inc.

K Number Device Name
K200115 Cavetto-SA Cervical Cage System
K201769 Cavetto [MAX] Cervical Cage System
K200927 Transept Cervical Plate System
K192248 Cortina™ [MAX] Lumbar Cage System
K182195 Arco™-SA Lumbar Cage System
K181590 Neurostructures Cavetto® [MAX] Cervical Cage System
K173082 Arco™-SA Lumbar Cage System
K180431 Cortina [MAX] Lumbar Cage System
K172320 Neurostructures Cavetto® Cervical Cage System
K173077 Cavetto-SA Cervical Cage System
Search all 15 clearances from Neurostructures, Inc. →