TiBow

TiBOW Trial, 28mm x 10mm, 12 Degree

Registry build 21.09.26
14manufacturers in China registered for this device type
81catalogue numbers in this listing
33510(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 TiBow
Listed by Life 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, Manufacturer
510(k) K170919
Record published 2019-11-07
Record revised 2025-07-14 (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

Catalogue Numbers

Catalogue numbers for TiBow
Catalogue number Size Status
60-1128-111X In distribution
129-1221 In distribution
60-1136-110X In distribution
129-327 In distribution
129-338 In distribution
129-333 In distribution
129-589 In distribution
60-1128-110X In distribution
60-1128-108X In distribution
60-1128-212X In distribution
129-335 In distribution
129-1216 In distribution
129-325 In distribution
114-351-2 In distribution
129-591 In distribution
60-1128-210X In distribution
129-1269 In distribution
129-1207 In distribution
114-351-3 In distribution
129-323 In distribution
60-1128-208X In distribution
129-1211 In distribution
129-332 In distribution
113-428 In distribution
129-1210 In distribution
129-334 In distribution
129-1213 In distribution
114-351-1 In distribution
60-1136-109X In distribution
129-1206 In distribution
129-324 In distribution
60-1136-108X In distribution
129-321 In distribution
60-1128-211X In distribution
129-1218 In distribution
129-339 In distribution
129-329 In distribution
129-1212 In distribution
129-590 In distribution
129-1214 In distribution
129-331 In distribution
129-1209 In distribution
129-330 In distribution
60-1128-109X In distribution
129-1278 In distribution
129-328 In distribution
129-1263 In distribution
129-1208 In distribution
149-068 In distribution
129-594 In distribution
60-1136-210X In distribution
60-1136-209X In distribution
129-1204 In distribution
129-320 In distribution
129-1219 In distribution
60-1128-112X In distribution
129-592 In distribution
129-1217 In distribution
129-1222 In distribution
60-1128-209X In distribution
129-1205 In distribution
129-326 In distribution
129-1215 In distribution
129-336 In distribution
60-1136-211X In distribution
129-593 In distribution
129-1220 In distribution
114-325 In distribution
60-1136-208X In distribution
114-351-5 In distribution
149-069 In distribution
60-1136-111X In distribution
129-337 In distribution
129-322 In distribution
129-1264 In distribution
129-1223 In distribution
129-1268 In distribution
114-351-4 In distribution
129-1203 In distribution
60-1136-212X In distribution
60-1136-112X 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
K261430 2026-07-28
K260837 2026-05-12
K253748 2026-01-23
K251502 2025-07-07
K250373 2025-04-09
K243668 2025-01-23
K242826 2024-10-08
K232611 2023-11-30
K223430 2023-05-04
K221806 2022-12-05
K213417 2022-09-29
K212520 2021-10-08
K210061 2021-04-30
K203361 2021-03-17
K201721 2020-09-04
K201500 2020-08-04
K193521 2020-02-06
K193258 2020-01-31
K190721 2019-11-14
K190488 2019-07-23
K191005 2019-06-13
K181625 2018-12-11
K182470 2018-11-26
K172105 2018-02-02
K173182 2017-12-20
K170919 2017-08-03
K153400 2016-03-07
K133717 2014-09-19
K131077 2013-07-17
K130630 2013-06-13
K121116 2012-05-08
K111569 2011-07-06
K080411 2008-05-15

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