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

Neurostructures Cavetto® [MAX] Cervical Cage System

K Number: K181590 · Decision Nov 8, 2018
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
15
Review Days
143

Basic Information

Device Name
Neurostructures Cavetto® [MAX] Cervical Cage System
K Number
K181590
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neurostructures, Inc.
Date Received
June 18, 2018
Decision Date
November 8, 2018
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ODP), 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
K173082 Arco™-SA Lumbar Cage System
K180431 Cortina [MAX] Lumbar Cage System
K172320 Neurostructures Cavetto® Cervical Cage System
K173077 Cavetto-SA Cervical Cage System
K171914 Cortina™ Lumbar Cage System
Search all 15 clearances from Neurostructures, Inc. →