EVOL®ha-D Lateral Interbody Fusion System

EVOLha-D is a lateral lumbar interbody fusion spacer made from PEEK-OPTIMA LT120 HA. Its body has two central bone-graft windows and upper and lower teeth that resist migration between the…

Registry build 21.09.26

EVOLha-D is a lateral lumbar interbody fusion spacer made from PEEK-OPTIMA LT120 HA. Its body has two central bone-graft windows and upper and lower teeth that resist migration between the vertebral bodies.

Tantalum beads embedded in the spacer make it visible under fluoroscopy. Different footprints, heights and lordotic angles accommodate the lateral disc-space anatomy.

Listed Item

EVOL®ha LATERAL DLIF CAGE 12x18x50X15 deg

Lateral Fusion Construct

The spacer is used with autogenous and/or allogeneic cancellous or corticocancellous graft and supplemental lumbosacral fixation. Its indication covers one or two adjacent lumbar levels from L2 to S1 in skeletally mature patients following at least six months of nonoperative treatment.

14manufacturers in China registered for this device type
88catalogue numbers in this listing
6510(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 EVOL®ha-D Lateral Interbody Fusion System
Listed by Cutting Edge Spine, United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K192497
Record published 2020-02-14

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, expiry date, manufacturing date
Storage Special storage condition: Store at room temperature

Catalogue Numbers

Catalogue numbers for EVOL®ha-D Lateral Interbody Fusion System
Catalogue number Size Status
HA501812-15 In distribution
HA602212-15 In distribution
HA552208-10 In distribution
HA551814-00 In distribution
HA501810-10 In distribution
HA602214-10 In distribution
HA601814-10 In distribution
HA452214-15 In distribution
HA602212-10 In distribution
HA602210-10 In distribution
HA602210-00 In distribution
HA601814-00 In distribution
HA451812-10 In distribution
HA452210-10 In distribution
HA602212-00 In distribution
HA552214-10 In distribution
HA551808-10 In distribution
HA602208-00 In distribution
HA601808-00 In distribution
HA502210-15 In distribution
HA502212-10 In distribution
HA601812-15 In distribution
HA501812-00 In distribution
HA451808-00 In distribution
HA501814-10 In distribution
HA502214-00 In distribution
HA551808-00 In distribution
HA601810-15 In distribution
HA502208-00 In distribution
HA451814-10 In distribution
HA501810-00 In distribution
HA551814-15 In distribution
HA601810-10 In distribution
HA601808-10 In distribution
HA551812-10 In distribution
HA502214-15 In distribution
HA501808-10 In distribution
HA452212-10 In distribution
HA552212-15 In distribution
HA502208-10 In distribution
HA552212-10 In distribution
HA452210-15 In distribution
HA602214-00 In distribution
HA452214-10 In distribution
HA452210-00 In distribution
HA552212-00 In distribution
HA452214-00 In distribution
HA552212-15 In distribution
HA501812-10 In distribution
HA452208-00 In distribution
HA451814-00 In distribution
HA502212-15 In distribution
HA601812-10 In distribution
HA551810-00 In distribution
HA502214-10 In distribution
HA602208-10 In distribution
HA451814-15 In distribution
HA452212-00 In distribution
HA552210-10 In distribution
HA552210-00 In distribution
HA601810-00 In distribution
HA502210-10 In distribution
HA502210-00 In distribution
HA552208-00 In distribution
HA552210-15 In distribution
HA601812-00 In distribution
HA451812-00 In distribution
HA601814-15 In distribution
HA551814-10 In distribution
HA501814-00 In distribution
HA551810-10 In distribution
HA551812-00 In distribution
HA602210-15 In distribution
HA502212-00 In distribution
HA451810-10 In distribution
HA451808-10 In distribution
HA452212-15 In distribution
HA552214-00 In distribution
HA501808-00 In distribution
HA451812-15 In distribution
HA501810-15 In distribution
HA452208-10 In distribution
HA602214-15 In distribution
HA451810-15 In distribution
HA451810-00 In distribution
HA501814-15 In distribution
HA551810-15 In distribution
HA551812-15 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
K200991 2020-05-13
K200552 2020-04-02
K192497 2020-01-06
K180891 2018-05-04
K150321 2015-07-13
K102957 2011-04-28

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