InterStim™ Micro SureScan™

INS 97810 Istm Micro Ssmri RC Eman US

Registry build 21.09.26
1manufacturer
1catalogue number

Who Else Makes It

Registered in Shanghai. One is registered as a contract manufacturer, able to build to a specification.

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

Record

Regulatory record for InterStim™ Micro SureScan™
Listed by Medtronic, Inc., United States
FDA product code EZW
Device type Stimulator, Electrical, Implantable, For Incontinence
Device class Class 3
Regulation 21 CFR 876.5270
Establishment Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) P080025
Record published 2020-08-10
Record revised 2025-10-09 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries serial number
Distribution end date 2025-10-07

Catalogue Numbers

Catalogue numbers for InterStim™ Micro SureScan™
Catalogue number Size Status
97810 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Interstim® Medtronic, Inc. 88
Neuspera SNM System Neuspera Medical, Inc. 49
Stimulator, Electrical, Implantable, For Incontinence Medtronic, Inc. 44
InterStim™ SureScan™ Medtronic, Inc. 13
Axonics Axonics Modulation Technologies, Inc. 10
Verify™ Medtronic, Inc. 5
InterStim iCon Medtronic, Inc. 4
Interstim® Twist-Lock Cable Medtronic, Inc. 2
InterStim™ Micro Medtronic, Inc. 1
Verify® External Neurostimulator Medtronic, Inc. 1
InterStim™ X 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
P240031 2026-08-21 Neuspera Sacral Neuromodulation (SNM) System Neuspera Medical, Inc.
P970004 2025-09-05 InterStim® Therapy System; Verify® Evaluation System Medtronic Neuromodulation
P170001 2023-01-11 VIRTIS SACRAL NEUROMODULATION SYSTEM Cirtec Medical
P180046 2022-01-04 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