TrellOss™-A

ALIF, Tray ALIF Insertion

Registry build 21.09.26
14manufacturers in China registered for this device type
77catalogue 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™-A
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) K193370
Record published 2020-06-24
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
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Width 32 to 36 mm; depth 24 to 27 mm; height 8 to 20 mm; angle 8 to 20 °

Catalogue Numbers

Catalogue numbers for TrellOss™-A
Catalogue number Size Status
308H3612 Width 36 mm In distribution
336H0816 In distribution
314H3618 Width 36 mm In distribution
332H1416 In distribution
308H3618 Width 36 mm In distribution
314H3218 Width 32 mm In distribution
332H0818 In distribution
336H0810 In distribution
332H1418 In distribution
314H3620 Width 36 mm In distribution
332H2016 In distribution
332H1412 In distribution
320H3216 Width 32 mm In distribution
320H3614 Width 36 mm In distribution
330H0003 In distribution
336H1420 In distribution
332H0814 In distribution
336H0812 In distribution
314H3612 Width 36 mm In distribution
336H0818 In distribution
308H3216 Width 32 mm In distribution
332H1410 In distribution
332H0816 In distribution
332H2018 In distribution
320H3618 Width 36 mm In distribution
336H2012 In distribution
336H0808 In distribution
300H2000 In distribution
336H1412 In distribution
330H0008 In distribution
314H3214 Width 32 mm In distribution
308H3210 Width 32 mm In distribution
336H2018 In distribution
300H1000 In distribution
320H3214 Width 32 mm In distribution
332H1414 In distribution
336H1410 In distribution
332H0812 In distribution
314H3210 Width 32 mm In distribution
330H0001 In distribution
336H2020 In distribution
308H3212 Width 32 mm In distribution
308H3220 Width 32 mm In distribution
314H3614 Width 36 mm In distribution
336H1416 In distribution
336H2016 In distribution
308H3218 Width 32 mm In distribution
320H3612 Width 36 mm In distribution
320H3220 Width 32 mm In distribution
332H2012 In distribution
308H3214 Width 32 mm In distribution
336H2014 In distribution
308H3208 Width 32 mm In distribution
300H2001 In distribution
314H3616 Width 36 mm In distribution
308H3608 Width 36 mm In distribution
308H3610 Width 36 mm In distribution
320H3212 Width 32 mm In distribution
320H3616 Width 36 mm In distribution
336H0820 In distribution
308H3614 Width 36 mm In distribution
320H3218 Width 32 mm In distribution
336H1418 In distribution
332H0808 In distribution
320H3620 Width 36 mm In distribution
314H3220 Width 32 mm In distribution
332H0810 In distribution
314H3212 Width 32 mm In distribution
332H2020 In distribution
314H3610 Width 36 mm In distribution
336H1414 In distribution
308H3616 Width 36 mm In distribution
332H2014 In distribution
308H3620 Width 36 mm In distribution
336H0814 In distribution
332H1420 In distribution
314H3216 Width 32 mm 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