Skip to content

Interstim® 367675

by Medtronic, Inc. 2 variants

Interstim® 367675 is a Class III device made by Medtronic, Inc., approved under FDA PMA P080025 on 14 Mar 2011 (1 earlier submission) and listed in FDA GUDID since 9 Jun 2017 (UDI-DI 20643169721238), active as of 23 Oct 2026. 5 FDA recalls are linked to it.

Active United States. Also listed in GUDID (US).

PMA

Valid until

No expiry

PMA approval is not time-limited

FDA recalls

3 ongoing

This device is named in the recall

Documents

PMA P080025

+1 more

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20643169721238 UDI-DI Date9 Jun 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA PMAAPPR from GUDID Approved NumberP080025 Date14 Mar 2011DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA PMA P080025 decided 14 Mar 2011 Active· +1 more in the status table
  • FDA GUDID UDI-DI 20643169721238 listed 9 Jun 2017 Listed

Recalls

7 recalls · 3 ongoing · FDA

    • Ongoing Z-1704-2025 FDA Class II initiated 3 Apr 2025

    Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing speed than prior handsets. An inability to connect may cause the therapy to stop being delivered and a system error will be displayed. Patient may experience return of underlying disease symptoms (e.g. overactive bladder, urinary retention, or fecal incontinence) based on their response to stimulation during the evaluation period.

    • Ongoing Z-0372-2025 FDA Class II initiated 18 Sep 2024 on shared PMA P080025

    The Wireless Rechargers in the kits may be unable to enter a recharging session upon first use.

    • Ongoing Z-2365-2023 FDA Class II initiated 6 Jul 2023

    Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.

    • Terminated Z-0998-2022 FDA Class II initiated 28 Feb 2022

    There is a software anomaly with the InterStim X Clinician software application with results in the data entered in the Patient Information fields not e retained and a " Data Lost" notification being displayed.

    • Terminated Z-1147-2015 FDA Class II initiated 9 Jan 2015 on shared PMA P080025

    Current labeling indicates that cycling improves device longevity in every programming scenario. However, enabling cycling at certain parameter settings may decrease the device battery longevity. With cycling enabled, longevity estimate displayed on the Model 8840Programmer may be inaccurate.

    • Terminated Z-0037-2008 FDA Unclassified (pre-2012) initiated 25 Jun 2007

    A software issue may cause a lower than expected battery capacity estimate when evaluating an InterStim II Implantable Neurostimulator (model 3058) with an N'Vision Clinician Programmer(Model 8840) before implant .

    • Terminated Z-0040-2008 FDA Unclassified (pre-2012) initiated 25 Jun 2007

    Software issue may cause false low battery alert to be displayed when interrogating an Interstim Implantable Neurostimulator (Model 3023) with an N'Vision Clinician Programmer (Model 8840), or with an Inter Stim iCon Patient Programmer (Model 3037).

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Timeline

10 dated events

  1. Approved FDA PMA P970004
  2. Recall initiated FDA recalls Z-0037-2008
  3. Recall initiated FDA recalls Z-0040-2008
  4. Approved FDA PMA P080025
  5. Recall initiated FDA recalls Z-1147-2015
  6. Listed FDA GUDID 20643169721238
  7. Recall initiated FDA recalls Z-0998-2022
  8. Recall initiated FDA recalls Z-2365-2023
  9. Recall initiated FDA recalls Z-0372-2025
  10. Recall initiated FDA recalls Z-1704-2025

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Active

Specification

GUDID

Trade name
Interstim®
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
367675
Primary DI / UDI-DI
20643169721238
PMA number
FDA product code
EZW
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class III
Regulation number
876.5270
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrical-only medical device connection cable, reusable

Cleared under the same submission (P080025)

and 8 more cleared under P080025

Cleared under the same submission (P970004)

and 8 more cleared under P970004

Similar devices in this category

Other devices filed under Electrical-only medical device connection cable, reusable.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)