Cavetto

Trial With Handle Peak to Peak 12x14x05

Registry build 21.09.26
7manufacturers in China registered for this device type
75catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Shandong (2), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ODP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10
Shanghai Sanyou Medical Co., Ltd. Shanghai Shanghai Manufacturer 6

Record

Regulatory record for Cavetto
Listed by Neurostructures, Inc., United States
FDA product code ODP
Device type Intervertebral Fusion Device With Bone Graft, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
Record published 2016-01-11
Record revised 2020-02-24 (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
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Cavetto
Catalogue number Size Status
30-90-002-141606 In distribution
100018-16188 In distribution
30-90-006P-121405 In distribution
30-90-002-121408 In distribution
30-90-002-121407 In distribution
30-90-006-121407 In distribution
30-90-006P-141610 In distribution
100018-12145 In distribution
30-90-006P-121410 In distribution
30-90-002-141609 In distribution
30-90-006-141607 In distribution
30-90-010 In distribution
30-90-006-141604 In distribution
100018-16186 In distribution
30-90-006P-161805 In distribution
100018-16184 In distribution
30-90-006P-141609 In distribution
30-90-002-141610 In distribution
30-90-006P-161806 In distribution
30-90-002-121406 In distribution
30-90-000 In distribution
100018-14168 In distribution
30-90-006P-141607 In distribution
30-90-004 In distribution
100018-12147 In distribution
30-90-000-001 In distribution
100018-16185 In distribution
30-90-002-141607 In distribution
30-90-006P-121409 In distribution
30-90-006-121409 In distribution
30-90-006P-121407 In distribution
100018-14169 In distribution
100018-16189 In distribution
30-90-002-121410 In distribution
30-90-002-121409 In distribution
100018-141610 In distribution
100018-14167 In distribution
100018-14164 In distribution
30-90-002-141605 In distribution
100018-12149 In distribution
30-90-006-121406 In distribution
30-90-006-121404 In distribution
30-90-006-141609 In distribution
30-90-006P-141604 In distribution
100018-16187 In distribution
30-90-006-141606 In distribution
100018-121410 In distribution
100018-12148 In distribution
30-90-002-141608 In distribution
100018-12144 In distribution
30-90-006-141608 In distribution
100018-12146 In distribution
30-90-005 In distribution
30-90-006-141605 In distribution
100018-14165 In distribution
30-90-006P-141608 In distribution
30-90-006P-141605 In distribution
30-90-006P-161808 In distribution
30-90-006P-141606 In distribution
30-90-002-141604 In distribution
30-90-006P-121404 In distribution
30-90-006P-161807 In distribution
100018-14166 In distribution
30-90-006-121408 In distribution
30-90-006-141610 In distribution
30-90-006P-121406 In distribution
30-90-002-121404 In distribution
30-90-006P-161804 In distribution
30-90-001 In distribution
30-90-006-121410 In distribution
30-90-007-014 In distribution
30-90-006-121405 In distribution
30-90-002-121405 In distribution
30-90-006P-161809 In distribution
30-90-006P-121408 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Latitude-C AM™ Cervical Interbody Fusion System Degen Medical 1,529
IdentiTi Alphatec Spine, Inc. 1,390
Zavation Zavation 1,357
IVA Cage Ti Diomedical Co., Ltd. 1,202
Latitude-C Cervical Interbody Spacer System Degen Medical 1,185
Peridot Anterior Cervical Intervertebral Body Fusion System Gbs Commonwealth Co., Ltd. 1,056
Aleutian® Interbody Systems VB Spine LLC 1,017
Valeo Spacer System Sintx Technologies Inc. 918
Cascadia™ Interbody System VB Spine LLC 823
CoRoent Nuvasive, Inc. 815
Tyber Medical Tyber Medical 740
Matisse Anterior Cervical Interbody Fusion Cage System CTL Medical Corporation 577

Showing 12 of 938. All products under Intervertebral Fusion Device With Bone Graft, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201769 2020-09-03
K181590 2018-11-08
K172320 2018-02-26

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