MyndStep Foot Drop Stimulator
MyndStep Foot Drop Stimulator (800102) is a Class II device made by Myndtec, Inc., cleared under FDA 510(k) K202110 on 5 Nov 2021 and listed in FDA GUDID since 16 Sep 2022 (UDI-DI 00692520001027), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00692520001027 | Date16 Sep 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK202110 | Date5 Nov 2021 | StatusActive |
Official records
- AccessGUDID record 00692520001027
- FDA 510(k) database K202110
Across registries
- FDA 510(k) K202110 decided 5 Nov 2021 Active
- FDA GUDID UDI-DI 00692520001027 listed 16 Sep 2022 Listed
Timeline
- Cleared FDA 510(k) K202110
- Listed FDA GUDID 00692520001027
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MyndStep
- Generic name
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Model / Ref / Catalog
- MyndStep Foot Drop Stimulator, 800102
- Primary DI / UDI-DI
- 00692520001027
- 510(k) Number
- FDA product code
- GZI, IPF
- GMDN term
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Device class
- Class II
- Regulation number
- 882.5810, 890.5850
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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Other devices filed under FDA product code GZI (Stimulator, Neuromuscular, External Functional).
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- MODIFICATION TO HANDMASTER by Ness-Neuromuscular Electrical Stimulation Systems
- RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053 by Restorative Therapies, Inc.