Cortina

BN PLIF Cage, 4 Deg-Lordotic 25mmx9mmx10mm

Registry build 21.09.26
14manufacturers in China registered for this device type
140catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for Cortina
Listed by Neurostructures, Inc., United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Record published 2016-01-11
Record revised 2020-02-24 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Cortina
Catalogue number Size Status
31-90-006-28091004 In distribution
100198-250910 In distribution
31-90-006-28091000 In distribution
31-90-006-20091204 In distribution
31-90-006-31090700 In distribution
31-90-006-20090900 In distribution
31-90-006-31091104 In distribution
31-90-002-25091200 In distribution
31-90-006-28091100 In distribution
31-90-006-28090900 In distribution
100198-250912 In distribution
100035-310913 In distribution
31-90-006-31091304 In distribution
100035-280913 In distribution
100198-280907 In distribution
100035-280907 In distribution
100198-280910 In distribution
31-90-006-25090704 In distribution
31-90-006-25091300 In distribution
31-90-006-20090804 In distribution
31-90-006-20090704 In distribution
100198-200907 In distribution
100198-280912 In distribution
100035-310907 In distribution
31-90-006-20091100 In distribution
31-90-006-28090700 In distribution
100035-250913 In distribution
31-90-006-20091400 In distribution
31-90-006-25090800 In distribution
31-90-006-28091304 In distribution
100035-280912 In distribution
31-90-006-251090700 In distribution
31-90-006-31090900 In distribution
100035-310911 In distribution
31-90-006-20090904 In distribution
100035-200910 In distribution
31-90-006-31091300 In distribution
31-90-002-20091000 In distribution
31-90-006-28091200 In distribution
31-90-006-31091400 In distribution
31-90-006-20090700 In distribution
100198-310912 In distribution
31-90-006-28090904 In distribution
100035-250911 In distribution
100198-280915 In distribution
31-90-006-31091100 In distribution
100035-280911 In distribution
100198-250915 In distribution
31-90-006-25091100 In distribution
100035-310914 In distribution
100035-200911 In distribution
100035-280914 In distribution
100198-200914 In distribution
100198-310910 In distribution
100035-250912 In distribution
100035-200912 In distribution
100035-310912 In distribution
31-90-006-28091300 In distribution
100198-310908 In distribution
100198-280908 In distribution
100035-280908 In distribution
31-90-006-31090804 In distribution
31-90-006-25091404 In distribution
100035-250914 In distribution
31-90-006-20090800 In distribution
31-90-006-25091104 In distribution
31-90-006-25091304 In distribution
100198-200911 In distribution
31-90-002-25090900 In distribution
100198-280913 In distribution
100198-310913 In distribution
100035-310908 In distribution
100198-280911 In distribution
31-90-006-31091404 In distribution
100198-310911 In distribution
31-90-006-20091200 In distribution
31-90-006-31091004 In distribution
100198-310907 In distribution
31-90-006-20091404 In distribution
31-90-006-25090904 In distribution
100198-250911 In distribution
100035-200909 In distribution
100198-280914 In distribution
31-90-006-28091204 In distribution
31-90-002-25091000 In distribution
100035-250908 In distribution
31-90-006-20091004 In distribution
31-90-006-20091104 In distribution
100198-250914 In distribution
100198-200912 In distribution
31-90-006-25090804 In distribution
100198-280909 In distribution
31-90-006-25091204 In distribution
31-90-006-20091304 In distribution
100198-250913 In distribution
31-90-006-25091000 In distribution
100035-310910 In distribution
100198-310909 In distribution
31-90-006-28091400 In distribution
100035-200914 In distribution
31-90-006-25091400 In distribution
31-90-006-31091204 In distribution
31-90-002-20090900 In distribution
31-90-006-20091300 In distribution
31-90-006-31091200 In distribution
100035-200907 In distribution
31-90-006-25091004 In distribution
31-90-002-20091200 In distribution
100198-310914 In distribution
100198-200909 In distribution
31-90-006-25090900 In distribution
31-90-006-28091404 In distribution
100035-200908 In distribution
100035-250909 In distribution
100198-200913 In distribution
31-90-006-31090904 In distribution
31-90-006-31090800 In distribution
31-90-006-28091104 In distribution
31-90-006-25091200 In distribution
100035-250910 In distribution
31-90-006-28090704 In distribution
31-90-006-28090800 In distribution
31-90-010-09 In distribution
100198-250907 In distribution
100035-250907 In distribution
31-90-006-31090704 In distribution
100198-250908 In distribution
100198-250909 In distribution
100198-200910 In distribution
31-90-002-20091100 In distribution
100035-280909 In distribution
31-90-006-31091000 In distribution
100035-200913 In distribution
31-90-002-25091100 In distribution
31-90-006-28090804 In distribution
100035-280910 In distribution
100035-310909 In distribution
100198-200908 In distribution
31-90-001-09 In distribution
31-90-006-20091000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K192248 2019-11-25
K180431 2018-03-22
K171914 2017-10-25

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer