FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Silk Voice
K Number: K180631
·
Decision Nov 8, 2018
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
16
Applicant Total
2
Review Days
244
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Basic Information
- Device Name
- Silk Voice
- K Number
- K180631
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.3620
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Sofregen Medical, Inc.
- Date Received
- March 9, 2018
- Decision Date
- November 8, 2018
- Product Code
- MIX
- 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 |
|---|---|---|---|
| MIX | System, Vocal Cord Medialization | FDA class 2 | Ear, Nose, Throat |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (MIX), ordered by most recent decision date.
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VOCALIS AND VOCALIS SM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Other Clearances by Sofregen Medical, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K172545 | SERI Contour | Sep 22, 2017 | Substantially Equivalent |