TrellOss™

Inline Articulating Inserter Inner Shaft

Registry build 21.09.26
14manufacturers in China registered for this device type
85catalogue numbers in this listing
4510(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 TrellOss™
Listed by Nexxt Spine LLC, 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 Contract manufacturer, Complaint-file establishment, Manufacturer
510(k) K191408
Record published 2019-08-07
Record revised 2023-04-04 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Sizes Angle 0 to 10 °; height 7 to 16 mm; width 9 to 10 mm; length 22 to 32 mm

Catalogue Numbers

Catalogue numbers for TrellOss™
Catalogue number Size Status
206M2811 Angle 10 ° In distribution
207M3013 Angle 0 ° In distribution
208M3015 Angle 6 ° In distribution
206M2815 Angle 10 ° In distribution
208M2211 Angle 6 ° In distribution
204M3210 Angle 0 ° In distribution
207M2213 Angle 0 ° In distribution
207M3015 Angle 0 ° In distribution
204M3211 Length 32 mm In distribution
204M2812 Length 28 mm In distribution
200M5110 In distribution
207M2207 Angle 0 ° In distribution
208M2215 Angle 6 ° In distribution
206M3214 Angle 10 ° In distribution
230M0018 In distribution
206M3213 Length 32 mm In distribution
207M2610 Angle 0 ° In distribution
207M3007 Angle 0 ° In distribution
200M3100 In distribution
206M2812 Length 28 mm In distribution
230M0001 In distribution
207M2209 Angle 0 ° In distribution
206M2816 Length 28 mm In distribution
204M2815 Angle 0 ° In distribution
207M2616 Angle 0 ° In distribution
206M3208 Angle 10 ° In distribution
204M2807 Angle 0 ° In distribution
206M3215 Height 15 mm In distribution
207M3011 Angle 0 ° In distribution
204M3209 Length 32 mm In distribution
200M2111 In distribution
200M5101 In distribution
230M0013 In distribution
207M3009 Angle 0 ° In distribution
208M3009 Angle 6 ° In distribution
200M4103 In distribution
208M3013 Angle 6 ° In distribution
204M3216 Angle 0 ° In distribution
206M2810 Length 28 mm In distribution
200M8100 In distribution
207M2612 Angle 0 ° In distribution
207M2608 Angle 0 ° In distribution
200M1113 In distribution
100N3101 In distribution
207M2215 Angle 0 ° In distribution
208M2614 Angle 6 ° In distribution
207M2211 Angle 0 ° In distribution
204M2811 Angle 0 ° In distribution
204M3207 Length 32 mm In distribution
230M0012 In distribution
204M3213 Length 32 mm In distribution
206M3210 Angle 10 ° In distribution
207M2614 Angle 0 ° In distribution
206M2809 Angle 10 ° In distribution
204M2809 Angle 0 ° In distribution
204M2808 Length 28 mm In distribution
208M3011 Angle 6 ° In distribution
200M0110 In distribution
208M2209 Angle 6 ° In distribution
204M3208 Angle 0 ° In distribution
204M2810 Length 28 mm In distribution
204M3215 Length 32 mm In distribution
206M3211 Length 32 mm In distribution
206M3212 Angle 10 ° In distribution
206M2814 Length 28 mm In distribution
204M3214 Angle 0 ° In distribution
206M2808 Length 28 mm In distribution
208M2608 Angle 6 ° In distribution
208M2610 Angle 6 ° In distribution
204M2814 Length 28 mm In distribution
206M3209 Length 32 mm In distribution
208M2616 Angle 6 ° In distribution
206M3216 Width 10 mm In distribution
200M6103 In distribution
230M0017 In distribution
200M1111 In distribution
206M2813 Angle 10 ° In distribution
230M0003 In distribution
230M0015 In distribution
204M2816 Length 28 mm In distribution
200M1100 In distribution
208M2213 Angle 6 ° In distribution
204M2813 Angle 0 ° In distribution
204M3212 Angle 0 ° In distribution
208M2612 Angle 6 ° 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
K200969 2020-05-21
K193370 2020-01-21
K192687 2020-01-09
K191408 2019-07-10

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