TELIGEN System Peripheral Motor Nerve Stimulation Indications
FDA 510(k) clearance K223438 · decided 2023-02-10
Clearance details
- K-number
- K223438
- Device name
- TELIGEN System Peripheral Motor Nerve Stimulation Indications
- Applicant
- Medos International SARL
- Decision
- Substantially Equivalent
- Date received
- 2022-11-14
- Decision date
- 2023-02-10
- Days to decision
- 88 days
- Clearance type
- Traditional
- Product code
- PDQ
- Device class
- 2
- Regulation number
- 874.1820
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Le Locle, CH
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.