FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SEVIIN SURFACE REPLACEMENT SHOULDER
K Number: K130635
·
Decision Aug 26, 2013
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
70
Applicant Total
3
Review Days
168
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Basic Information
- Device Name
- SEVIIN SURFACE REPLACEMENT SHOULDER
- K Number
- K130635
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3690
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ingen Orthopedics, LLC
- Date Received
- March 11, 2013
- Decision Date
- August 26, 2013
- Product Code
- HSD
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- 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 |
|---|---|---|---|
| HSD | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | FDA class 2 | Orthopedic |
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