ShurFit Interbody Device

Wide PLIF Cage Peek 15 degree 22 x 10 x 14mm

Registry build 21.09.26
14manufacturers in China registered for this device type
170catalogue numbers in this listing
2510(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 ShurFit Interbody Device
Listed by Precision Spine, 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
Establishment Manufacturer
510(k) K092193
Record published 2019-04-26
Record revised 2020-02-24 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Over the counter Yes
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for ShurFit Interbody Device
Catalogue number Size Status
26-250800-13 In distribution
26-251005-08 In distribution
26-250805-08 In distribution
PLIF25-08P In distribution
ALIF1539-17P In distribution
26-250805-10 In distribution
ALIF1526-13P In distribution
26-221000-11 In distribution
21-1002-CD1 In distribution
ALIF1539-11P In distribution
26-251010-16 In distribution
ALIF0832-09P In distribution
44-3015-10 In distribution
26-220805-09 In distribution
26-220800-11 In distribution
ALIF0832-21P In distribution
PLIF25-15P In distribution
ALIF0832-19P In distribution
26-250810-12 In distribution
26-220805-16 In distribution
ALIF0826-19P In distribution
26-221015-14 In distribution
07-2909 In distribution
26-251000-07 In distribution
TLIF24-10P In distribution
44-3505-08 In distribution
44-2510-14 In distribution
ALIF1539-19P In distribution
26-220815-13 In distribution
44-3510-12 In distribution
26-221010-12 In distribution
ALIF1532-11P In distribution
44-2515-14 In distribution
07-2916 In distribution
44-3015-12 In distribution
26-250800-08 In distribution
26-251000-16 In distribution
ALIF1539-13P In distribution
26-221010-16 In distribution
26-250805-16 In distribution
PLIF22-16P In distribution
26-251000-11 In distribution
26-221000-16 In distribution
TLIF24-08P In distribution
26-220815-14 In distribution
ALIF0826-09P In distribution
26-250800-15 In distribution
44-3015-14 In distribution
07-2907 In distribution
TLIF24-10 In distribution
07-2912 In distribution
ALIF0832-15P In distribution
ALIF0826-13P In distribution
ALIF0826-15P In distribution
26-250805-12 In distribution
PLIF22-14P In distribution
ALIF0839-15P In distribution
26-220805-08 In distribution
26-220800-16 In distribution
TLIF24-14 In distribution
26-221015-15 In distribution
38-2915 In distribution
26-220800-12 In distribution
26-220810-11 In distribution
PLIF25-14P In distribution
26-220805-12 In distribution
ALIF1526-17P In distribution
26-250810-11 In distribution
ALIF1526-15P In distribution
ALIF0839-09P In distribution
26-250805-13 In distribution
07-2914 In distribution
26-250805-11 In distribution
26-220810-13 In distribution
ALIF1532-21P In distribution
44-3505-12 In distribution
ALIF1532-17P In distribution
26-250800-09 In distribution
44-2505-10 In distribution
26-250800-12 In distribution
26-251005-09 In distribution
ALIF0832-17P In distribution
ALIF0839-19P In distribution
44-3010-14 In distribution
TLIF24-09P In distribution
44-2505-12 In distribution
TLIF30-10P In distribution
TLIF24-16 In distribution
26-221000-13 In distribution
26-220800-07 In distribution
ALIF1532-13P In distribution
TLIF30-12P In distribution
38-2911 In distribution
26-220805-11 In distribution
PLIF25-13P In distribution
ALIF1532-19P In distribution
26-250800-07 In distribution
ALIF0839-13P In distribution
26-251015-15 In distribution
26-250810-09 In distribution
26-220810-14 In distribution
26-220815-16 In distribution
26-220810-15 In distribution
44-3005-12 In distribution
44-3515-12 In distribution
TLIF24-11P In distribution
44-3505-14 In distribution
ALIF0832-13P In distribution
38-2913 In distribution
38-2910 In distribution
TLIF30-16 In distribution
26-221015-12 In distribution
26-221000-15 In distribution
38-2912 In distribution
26-220815-15 In distribution
26-251005-16 In distribution
ALIF0826-11P In distribution
07-2911 In distribution
26-251010-14 In distribution
26-221015-16 In distribution
TLIF30-14 In distribution
TLIF30-09P In distribution
26-250805-15 In distribution
26-220800-09 In distribution
TLIF24-14P In distribution
07-2913 In distribution
44-3505-10 In distribution
07-2908 In distribution
ALIF0826-21P In distribution
PLIF25-12P In distribution
26-221005-15 In distribution
26-251010-15 In distribution
TLIF24-06P In distribution
26-250800-14 In distribution
26-250815-14 In distribution
ALIF0839-11P In distribution
44-3010-10 In distribution
TLIF30-08P In distribution
44-2515-12 In distribution
26-221015-13 In distribution
ALIF1539-15P In distribution
PLIF22-11P In distribution
44-2505-08 In distribution
ALIF1526-11P In distribution
26-250810-15 In distribution
ALIF1526-19P In distribution
PLIF22-15P In distribution
26-220815-11 In distribution
26-221005-10 In distribution
TLIF24-16P In distribution
44-3515-10 In distribution
26-250810-13 In distribution
ALIF0839-17P In distribution
TLIF30-10 In distribution
44-3510-14 In distribution
ALIF1532-15P In distribution
TLIF24-12 In distribution
26-250810-16 In distribution
ALIF0826-17P In distribution
26-221010-14 In distribution
26-250800-16 In distribution
PLIF22-13P In distribution
26-220800-14 In distribution
26-220805-10 In distribution
ALIF1526-21P In distribution
PLIF25-16P In distribution
TLIF30-07P In distribution
26-221005-13 In distribution
26-220800-10 In distribution
38-2908 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
K212075 2021-12-08
K171657 2017-08-11

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