FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
StimQ Peripheral Nerve Stimulator (PNS) System
K Number: K152178
·
Decision Mar 11, 2016
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
23
Applicant Total
1
Review Days
220
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Basic Information
- Device Name
- StimQ Peripheral Nerve Stimulator (PNS) System
- K Number
- K152178
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5870
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Stimq, LLC
- Date Received
- August 4, 2015
- Decision Date
- March 11, 2016
- Product Code
- GZF
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GZF | Stimulator, Peripheral Nerve, Implanted (Pain Relief) | FDA class 2 | Neurology |
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