Endoskeleton® TAS nanoLOCK® Surface Technology

Interbody Fusion Device 12 Degree Standard 14mm

Registry build 21.09.26
3manufacturers in China registered for this device type
48catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shandong (2), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OVD
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
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for Endoskeleton® TAS nanoLOCK® Surface Technology
Listed by Medtronic Sofamor Danek, Inc., United States
FDA product code OVD
Device type Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
510(k) K141953
Record published 2016-12-15
Record revised 2025-07-14 (version 8)

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
Sizes Depth 21 to 27 mm; angle 7 to 12 °; width 32 to 40 mm; height 10 to 17 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Endoskeleton® TAS nanoLOCK® Surface Technology
Catalogue number Size Status
2307-0312-N Depth 27 mm In distribution
2312-0312-N width(MLxAP), 40 x 27, mm In distribution
2312-0315-N Angle 12 ° In distribution
2307-0213-N Depth 24 mm In distribution
2307-0115-N Width 32 mm In distribution
2312-0114-N Width 32 mm In distribution
2312-0212-N Width 36 mm In distribution
2312-0112-N width(MLxAP), 32 x 21, mm In distribution
2312-0113-N Angle 12 ° In distribution
2312-0314-N width(MLxAP), 40 x 27, mm In distribution
2312-0311-N Depth 27 mm In distribution
2312-0116-N Angle 12 ° In distribution
2307-0116-N width(MLxAP), 32 x 21, mm In distribution
2312-0316-N Width 40 mm In distribution
2307-0315-N Depth 27 mm In distribution
2307-0211-N Width 36 mm In distribution
2307-0212-N width(MLxAP), 36 x 24, mm In distribution
2312-0310-N Depth 27 mm In distribution
2307-0117-N width(MLxAP), 32 x 21, mm In distribution
2307-0314-N Depth 27 mm In distribution
2312-0217-N Depth 24 mm In distribution
2307-0214-N Width 36 mm In distribution
2307-0316-N Width 40 mm In distribution
2307-0113-N width(MLxAP), 32 x 21, mm In distribution
2312-0211-N Depth 24 mm In distribution
2307-0111-N Depth 21 mm In distribution
2312-0110-N Depth 21 mm In distribution
2312-0210-N Width 36 mm In distribution
2307-0313-N width(MLxAP), 40 x 27, mm In distribution
2307-0317-N Width 40 mm In distribution
2312-0111-N Depth 21 mm In distribution
2307-0311-N Width 40 mm In distribution
2307-0310-N Angle 7 ° In distribution
2312-0214-N Width 36 mm In distribution
2307-0112-N width(MLxAP), 32 x 21, mm In distribution
2307-0215-N Width 36 mm In distribution
2312-0213-N Width 36 mm In distribution
2312-0117-N Depth 21 mm In distribution
2312-0215-N width(MLxAP), 36 x 24, mm In distribution
2312-0216-N width(MLxAP), 36 x 24, mm In distribution
2307-0217-N Depth 24 mm In distribution
2307-0110-N Width 32 mm In distribution
2307-0216-N Angle 7 ° In distribution
2307-0114-N Angle 7 ° In distribution
2312-0115-N width(MLxAP), 32 x 21, mm In distribution
2307-0210-N Width 36 mm In distribution
2312-0313-N width(MLxAP), 40 x 27, mm In distribution
2312-0317-N width(MLxAP), 40 x 27, mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sirion Astura Medical 1,465
IdentiTi Alphatec Spine, Inc. 1,372
EL Capitan Astura Medical 1,205
Zavation Zavation 1,157
Brigade Nuvasive, Inc. 1,005
Solar™ Interbody Fusion System Degen Medical 899
Zavation F3D Corpectomy Zavation 730
ROI-A Ldr Spine USA 552
Avenue L Ldr Spine USA 524
Transcend Nanotec Alphatec Spine, Inc. 485
Endoskeleton® TL Hyperlordotic nanoLOCK® Surface Technology Titan Spine, LLC 462
Base Nuvasive, Inc. 462

Showing 12 of 241. All products under Intervertebral Fusion Device With Integrated Fixation, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121982 2012-07-26
K110063 2011-10-04
K091813 2009-11-17

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Endoskeleton® TAS nanoLOCK® Surface Technology
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Medtronic Sofamor Danek USA, Inc. 510(k) number 2021-09-02 Class II Packaging change control Engraving on implants may not match what is listed on the pouch labels. 10 units 2023-10-05
Medtronic Sofamor Danek USA, Inc. 510(k) number 2021-03-17 Class II Packaging process control The shelf box identifies a small device actually contains a large device, and the shelf box identifying a large device actually contains a small device. 11 devices 2023-05-03
Medtronic Sofamor Danek USA, Inc. 510(k) number 2021-03-17 Class II Packaging process control The shelf box identifies a small device actually contains a large device, and the shelf box identifying a large device actually contains a small device. 11 devices 2023-05-03

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