Sequoia®

23 catalogue numbers from 3313-055, listed by Zimmer Spine, Inc., United States, under Thoracolumbosacral Pedicle Screw System. 15 manufacturers in China are registered for this product code.

Registry build 21.09.26
15manufacturers in China registered for this device type
23catalogue numbers in this listing
13510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Shandong (3). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NKB
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
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

Showing 12 of 15. All 15 manufacturers in China registered for Thoracolumbosacral Pedicle Screw System

Record

Regulatory record for Sequoia®
Listed by Zimmer Spine, Inc., United States
FDA product code NKB
Device type Thoracolumbosacral Pedicle Screw System
Device class Class 2
Regulation 21 CFR 888.3070
Record published 2015-09-24
Record revised 2025-07-02 (version 7)

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
Sizes Outer diameter 4.5 to 8.5 mm; length 25 to 100 mm; lumen/inner diameter 5.5 mm

Catalogue Numbers

Catalogue numbers for Sequoia®
Catalogue number Size Status
3313-055 Outer Diameter 5.5 mm In distribution
3306-6560 Outer Diameter 6.5 mm In distribution
3306-5540 Length 40 mm In distribution
3306-4525 Length 25 mm In distribution
3356-2 In distribution
3313-090 Outer Diameter 5.5 mm In distribution
3360-055 In distribution
3313-060 Outer Diameter 5.5 mm In distribution
3360-075 In distribution
3306-6530 Length 30 mm In distribution
3306-7540 Outer Diameter 7.5 mm In distribution
3313-095 Outer Diameter 5.5 mm In distribution
3361-065 In distribution
3367-2 In distribution
3306-5555 Outer Diameter 5.5 mm In distribution
3310-50 Lumen/Inner Diameter 5.5 mm In distribution
3306-5545 Length 45 mm In distribution
3313-100 Length 100 mm In distribution
3306-8545 Outer Diameter 8.5 mm In distribution
3306-5535 Outer Diameter 5.5 mm In distribution
3313-075 Length 75 mm In distribution
3361-045 In distribution
3301-1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
The Jasper Spinal Fixation System Gbs Commonwealth Co., Ltd. 32,491
Invictus Alphatec Spine, Inc. 4,722
Vital Spinal Fixation System Highridge Medical, LLC 4,422
Innoverse Spinal System CG MedTech Co., Ltd. 4,240
4CIS® Chiron Spinal Fixation System Alpha AI Co., Ltd. 3,787
LnK Spinal Fixation System L&K Biomed Co., Ltd. 3,522
Hedjet System Medyssey Co., Ltd. 3,438
Anax™ 5.5 Spinal System CG MedTech Co., Ltd. 3,424
Mega Plus MIS Spine System BK Meditech Co., Ltd. 3,396
ReLine Nuvasive, Inc. 2,882
Nex-D2 Next Orthosurgical 2,765
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 2,386

Showing 12 of 1,490. All products under Thoracolumbosacral Pedicle Screw System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K150896 2015-08-31
K142752 2015-06-18
K133291 2013-12-17
K133086 2013-11-27
K132884 2013-11-25
K131980 2013-09-04
K123552 2013-04-19
K121671 2012-07-18
K113270 2011-12-16
K111301 2011-08-26
K100845 2010-09-21
K072183 2007-09-05
K042702 2004-11-23

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2016-02-12 Class II Process control Zimmer Biomet is initiating a Medical Device Correction Notice to provide updated cleaning and disinfecting instructions for use of the Instinct Java System (IFU reference: 046WAN0000T) and Universal Clamp System (IFU reference: SNA027-N-90 2506 2016-08-11
2016-02-12 Class II Process control Zimmer Biomet is initiating a Medical Device Correction Notice to provide updated cleaning and disinfecting instructions for use of the Instinct Java System (IFU reference: 046WAN0000T) and Universal Clamp System (IFU reference: SNA027-N-90 3484 2016-08-11

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