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

Cortina™ [MAX] Lumbar Cage System

K Number: K192248 · Decision Nov 25, 2019
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
15
Review Days
98

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Basic Information

Device Name
Cortina™ [MAX] Lumbar Cage System
K Number
K192248
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
August 19, 2019
Decision Date
November 25, 2019
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
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
K171914 Cortina™ Lumbar Cage System
Search all 15 clearances from Neurostructures, Inc. →