Proficient™ Posterior Cervical Spine System

Cannulated Extended-Tab Smooth-Shank Translational Screw, 4.2 mm × 22 mm

Registry build 21.09.26
4manufacturers in China registered for this device type
1,590catalogue numbers in this listing
3510(k) clearances naming this product code

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 Proficient™ Posterior Cervical Spine System
Listed by Spine Wave, Inc., United States
FDA product code NKG
Device type Posterior Cervical Screw System
Device class Class 2
Regulation 21 CFR 888.3075
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K162639
Record published 2017-03-29
Record revised 2025-07-14 (version 6)

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

Catalogue Numbers

Catalogue numbers for Proficient™ Posterior Cervical Spine System
Catalogue number Size Status
11-8789 In distribution
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Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Bridalveil Astura Medical 1,718
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
Perla ® Spineart SA 349

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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K181440 2018-07-30
K172594 2017-12-15
K162639 2017-02-07

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