Monolith

Monolith Endcap, 15x13mm Parallel Ø12

Registry build 21.09.26
3manufacturers in China registered for this device type
107catalogue numbers in this listing
6510(k) clearances naming this product code
1recall

Who Else Makes It

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

Chinese manufacturers registered for FDA product code MQP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for Monolith
Listed by Nuvasive, Inc., United States
FDA product code MQP
Device type Spinal Vertebral Body Replacement Device
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K151538
Record published 2016-05-23
Record revised 2025-06-11 (version 10)

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 Monolith
Catalogue number Size Status
5991435 In distribution
5991226 In distribution
5992747 In distribution
5991413 In distribution
5991243 In distribution
5991248 In distribution
5991241 In distribution
5995124 In distribution
5991234 In distribution
5992757 In distribution
5991218 In distribution
5991153 In distribution
5991443 In distribution
5991229 In distribution
5991235 In distribution
5991196 In distribution
5991445 In distribution
5991415 In distribution
5991441 In distribution
5991215 In distribution
5991247 In distribution
5991211 In distribution
5991244 In distribution
5991426 In distribution
5991431 In distribution
5991245 In distribution
5992537 In distribution
5991425 In distribution
5991427 In distribution
5995123 In distribution
D5995100 In distribution
5992297 In distribution
5995122 In distribution
5992535 In distribution
5991230 In distribution
5991411 In distribution
5992745 In distribution
5991428 In distribution
5991434 In distribution
5991424 In distribution
5991219 In distribution
5991232 In distribution
5991420 In distribution
5991432 In distribution
5991416 In distribution
5991438 In distribution
5991444 In distribution
5991225 In distribution
5991418 In distribution
5991437 In distribution
5991014 In distribution
5991440 In distribution
5991220 In distribution
5991221 In distribution
5992740 In distribution
5992295 In distribution
5991429 In distribution
5991410 In distribution
5992967 In distribution
5991422 In distribution
5991436 In distribution
5991236 In distribution
5991238 In distribution
5991439 In distribution
5991242 In distribution
5991214 In distribution
5992755 In distribution
5992290 In distribution
5991016 In distribution
5991414 In distribution
5991222 In distribution
5991446 In distribution
5991231 In distribution
5991449 In distribution
5991447 In distribution
5991224 In distribution
5991213 In distribution
5991175 In distribution
5991233 In distribution
5991412 In distribution
5991421 In distribution
5991212 In distribution
5991417 In distribution
5991448 In distribution
5992530 In distribution
5991423 In distribution
5992960 In distribution
5991216 In distribution
5992965 In distribution
5991174 In distribution
5995121 In distribution
5991246 In distribution
5991433 In distribution
5991223 In distribution
5991129 In distribution
5991237 In distribution
5991240 In distribution
5991419 In distribution
5991217 In distribution
5991227 In distribution
5991239 In distribution
5991210 In distribution
5991442 In distribution
5992750 In distribution
5991228 In distribution
5991430 In distribution
5991249 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CoRoent Nuvasive, Inc. 1,514
Capri™ Corpectomy Cage System VB Spine LLC 1,509
Aleutian® Interbody Systems VB Spine LLC 1,189
Fortify Globus Medical, Inc. 866
Matrixx System Nexxt Spine LLC 748
Ascend Alphatec Spine, Inc. 555
Zavation VBR Trial Zavation 548
Verte-Stack® Spinal System Medtronic Sofamor Danek, Inc. 484
Timberline® Lateral Interbody Fusion System Biomet Spine 470
Timberline Lateral Fusion System Biomet Spine 459
Novel Alphatec Spine, Inc. 447
Hawkeye™ Vertebral Body Replacement (VBR) Choice Spine, LP 368

Showing 12 of 683. All products under Spinal Vertebral Body Replacement Device

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K142205 2015-02-20
K090176 2009-04-27
K052210 2005-12-12
K043405 2005-02-07
K032476 2003-11-13
K023319 2003-03-04

Recalls

1 of these is 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
2022-11-10 Class II Device Design Potential that insert will be unable to disengage from the vertebral body replacement device/implant 2,031 devices

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