MUSTmini Straght Rod

MUST MINI Rod CoCr ø3.5 x 100 mm

Registry build 21.09.26
4manufacturers in China registered for this device type
34catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (1), Shandong (1), Fujian (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NKG
Manufacturer City Province Registered as Device types
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Record

Regulatory record for MUSTmini Straght Rod
Listed by Medacta International SA, Switzerland
FDA product code NKG
Device type Posterior Cervical Screw System
Device class Class 2
Regulation 21 CFR 888.3075
Establishment Specification developer, Repacker / relabeller, Private-label distributor, Complaint-file establishment, Manufacturer, Exporter
510(k) K190631
Record published 2021-10-25
Record revised 2024-09-17 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for MUSTmini Straght Rod
Catalogue number Size Status
03.75.593 In distribution
03.75.633 In distribution
03.75.632 In distribution
03.75.639 In distribution
03.75.648 In distribution
03.75.695 In distribution
03.75.645 In distribution
03.75.595 In distribution
03.75.691 In distribution
03.75.647 In distribution
03.75.644 In distribution
03.75.646 In distribution
03.75.698 In distribution
03.75.649 In distribution
03.75.597 In distribution
03.75.643 In distribution
03.75.697 In distribution
03.75.634 In distribution
03.75.637 In distribution
03.75.642 In distribution
03.75.599 In distribution
03.75.696 In distribution
03.75.638 In distribution
03.75.596 In distribution
03.75.594 In distribution
03.75.641 In distribution
03.75.598 In distribution
03.75.636 In distribution
03.75.690 In distribution
03.75.640 In distribution
03.75.694 In distribution
03.75.635 In distribution
03.75.693 In distribution
03.75.692 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Bridalveil Astura Medical 1,718
Proficient™ Posterior Cervical Spine System Spine Wave, Inc. 1,590
Invictus Alphatec Spine, Inc. 1,538
Paeon Posterior Cervical Fixation System Aegis Spine 1,408
ReLine Nuvasive, Inc. 1,072
PathLoc-C Posterior Cervical Fixation System L&K Biomed Co., Ltd. 706
Cosy Signus Medizintechnik Gmbh 550
Yukon OCT Spinal System VB Spine LLC 451
Astra-OCT Spine System Spinecraft LLC 440
Symphony Medos International Sàrl 389
Medyssey Poseidon OCT Spinal Fixation System Medyssey Co., Ltd. 387
Infinity™ Occipitocervical Upper Thoracic System Medtronic Sofamor Danek, Inc. 375

Showing 12 of 336. All products under Posterior Cervical Screw System

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