Imola-Silverstone

Lordotic Implant Module Assy Imola Lateral IBF

Registry build 21.09.26
14manufacturers in China registered for this device type
103catalogue numbers in this listing

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 Imola-Silverstone
Listed by Altus 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
Premarket notification Exempt
Record published 2018-10-06
Record revised 2024-09-11 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Imola-Silverstone
Catalogue number Size Status
705-3017 In distribution
600-3104 In distribution
730-0001 In distribution
705-3006 In distribution
780-0012 In distribution
705-3014 In distribution
700-1040 In distribution
705-3011 In distribution
1000-0704 In distribution
600-4150 In distribution
1000-0703 In distribution
705-3018 In distribution
780-0002 In distribution
705-3010 In distribution
600-3105 In distribution
600-3103 In distribution
700-1100 In distribution
1000-0408 In distribution
707-1006 In distribution
790-0028F In distribution
705-3012 In distribution
707-1012 In distribution
780-0023 In distribution
1000-0736 In distribution
780-0011 In distribution
1000-0738 In distribution
1000-0731 In distribution
600-3130 In distribution
705-3016 In distribution
600-0014 In distribution
600-3110 In distribution
1000-0412 In distribution
600-3106 In distribution
780-0010 In distribution
705-2006 In distribution
705-2005 In distribution
790-0028 In distribution
780-0019 In distribution
706-0009 In distribution
700-1099 In distribution
707-1008 In distribution
600-3107 In distribution
600-4130 In distribution
1000-0210 In distribution
706-0013 In distribution
707-1017 In distribution
999-1000 In distribution
705-1007 In distribution
705-3013 In distribution
1000-0702 In distribution
700-0026 In distribution
600-3109 In distribution
1000-0410 In distribution
700-0030 In distribution
707-1009 In distribution
600-4110 In distribution
707-1007 In distribution
707-1010 In distribution
600-4090 In distribution
600-4000 In distribution
700-1026 In distribution
700-0022 In distribution
705-3009 In distribution
1000-0734 In distribution
707-1016 In distribution
705-3007 In distribution
1000-0735 In distribution
1000-0701 In distribution
780-0004 In distribution
705-3008 In distribution
790-0026 In distribution
700-0099 In distribution
707-1013 In distribution
790-0038 In distribution
705-3015 In distribution
600-3150 In distribution
600-2100 In distribution
700-1050 In distribution
1000-0732 In distribution
700-1030 In distribution
600-3090 In distribution
785-0022 In distribution
707-1014 In distribution
1000-0414 In distribution
780-0022 In distribution
705-2007 In distribution
780-0009 In distribution
790-0036 In distribution
780-0013 In distribution
1000-0733 In distribution
706-0011 In distribution
730-0003 In distribution
707-1015 In distribution
1000-0450 In distribution
790-0002 In distribution
706-0007 In distribution
1000-0705 In distribution
780-0005 In distribution
1000-0737 In distribution
730-0002 In distribution
707-1011 In distribution
707-1018 In distribution
700-1022 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

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