FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
WALKAIDE SYSTEM, MODELS 20-0100, 20-0310, 20-1000
K Number: K052329
·
Decision Sep 21, 2005
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
60
Applicant Total
3
Review Days
27
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Basic Information
- Device Name
- WALKAIDE SYSTEM, MODELS 20-0100, 20-0310, 20-1000
- K Number
- K052329
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 882.5810
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Innovative Neurotronics, Inc.
- Date Received
- August 25, 2005
- Decision Date
- September 21, 2005
- Product Code
- GZI
- 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 |
|---|---|---|---|
| GZI | Stimulator, Neuromuscular, External Functional | FDA class 2 | Neurology |
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