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

Cortina™ Lumbar Cage System

K Number: K171914 · Decision Oct 25, 2017
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
15
Review Days
121

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Basic Information

Device Name
Cortina™ Lumbar Cage System
K Number
K171914
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
June 26, 2017
Decision Date
October 25, 2017
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MAX), 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
K173077 Cavetto-SA Cervical Cage System
Search all 15 clearances from Neurostructures, Inc. →