FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SPIWay Endonasal Access Guide
K Number: K213153
·
Decision Oct 27, 2021
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
45
Applicant Total
4
Review Days
29
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Basic Information
- Device Name
- SPIWay Endonasal Access Guide
- K Number
- K213153
- Device Class
- FDA class 1
- Clearance Type
- Special
- Regulation Number
- 874.4780
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Spiway, LLC
- Date Received
- September 28, 2021
- Decision Date
- October 27, 2021
- Product Code
- LYA
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- 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 |
|---|---|---|---|
| LYA | Splint, Intranasal Septal | FDA class 1 | Ear, Nose, Throat |
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