Erisma®-LP MIS

Erisma LP MIS rods are components of a posterior pedicle-screw construct that stabilizes spinal segments during fusion. The system is designed for percutaneous fixation of the thoracic,…

Registry build 21.09.26

Erisma LP MIS rods are components of a posterior pedicle-screw construct that stabilizes spinal segments during fusion. The system is designed for percutaneous fixation of the thoracic, lumbar and sacral spine in skeletally mature patients.

The rods are medical-grade titanium alloy and come in straight or prebent forms within the wider system. The listed prelordosed rods are prebent members of that range.

Listed Item

MIS PRE-Lordosed ROD

Screw and Instrument Connections

Cannulated extended pedicle screws provide the rod’s anchoring points. Extended breakoff tabs support minimally invasive placement, and dedicated instruments accompany the posterior percutaneous system. Rod and screw diameters and lengths vary with patient anatomy.

15manufacturers in China registered for this device type
2catalogue numbers in this listing
6510(k) clearances naming this product code
1recall

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 Erisma®-LP MIS
Listed by Clariance, Inc., United States
FDA product code NKB
Device type Thoracolumbosacral Pedicle Screw System
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K162367
Record published 2024-12-02

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, manufacturing date
Sizes Outer diameter 5.5 mm; length 85 to 95 mm

Catalogue Numbers

Catalogue numbers for Erisma®-LP MIS
Catalogue number Size Status
13435095 Outer Diameter 5.5 mm In distribution
13435085 Outer Diameter 5.5 mm 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
K241863 2024-07-24
K240872 2024-04-26
K170163 2017-02-14
K162367 2016-10-27
K153326 2016-03-08
K120469 2012-08-13

Recalls

1 of these is Class III. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2019-07-01 Class III Use error Potential for the polyaxial screw to become disassembled during implant. 4,090 units distributed in the US 2020-07-09

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