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

Cavetto-SA Cervical Cage System

K Number: K173077 · Decision Feb 23, 2018
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
15
Review Days
147

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Basic Information

Device Name
Cavetto-SA Cervical Cage System
K Number
K173077
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neurostructures, Inc.
Date Received
September 29, 2017
Decision Date
February 23, 2018
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OVE), ordered by most recent decision date.

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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
K171914 Cortina™ Lumbar Cage System
Search all 15 clearances from Neurostructures, Inc. →