InterStim™ SureScan™

Lead 978A141 Istm Ssmri 2.16MM Eman Glbl

Registry build 21.09.26
1manufacturer
5catalogue numbers in this listing

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code QON
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31

Record

Regulatory record for InterStim™ SureScan™
Listed by Medtronic, Inc., United States
FDA product code QON
Device type Implanted Electrical Device Intended For Treatment Of Fecal Incontinence
Device class Class 3
Regulation 21 CFR 876.5270
Establishment Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) P080025
Record published 2024-01-22
Record revised 2026-02-25 (version 4)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number
Sizes Length 33 to 41 cm

Catalogue Numbers

Catalogue numbers for InterStim™ SureScan™
Catalogue number Size Status
978A141 Length 41.0 cm In distribution
978B133 Length 33.0 cm In distribution
978B133 Length 33.0 cm In distribution
978A133 Length 33.0 cm In distribution
978A141 Length 41.0 cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Axonics Axonics Modulation Technologies, Inc. 22
Implanted Electrical Device Intended For Treatment Of Fecal Incontinence Medtronic, Inc. 6
Verify™ Medtronic, Inc. 4
InterStim™ X Medtronic, Inc. 1
InterStim™ Micro SureScan™ MRI Medtronic, Inc. 1
Interstim® II Medtronic, Inc. 1

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P080025 2024-12-13 InterStim Therapy System, Verify Evaluation System Medtronic Neuromodulation
P190006 2023-03-02 Axonics Sacral Neuromodulation System Boston Scientific Corporation

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