FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Akros FibuLink Syndesmosis Repair Kit
K Number: K173550
·
Decision Dec 14, 2017
Classifications
1
FEI Numbers
272
Registration Numbers
272
Same Product Code
92
Applicant Total
3
Review Days
28
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Basic Information
- Device Name
- Akros FibuLink Syndesmosis Repair Kit
- K Number
- K173550
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Akros Medical
- Date Received
- November 16, 2017
- Decision Date
- December 14, 2017
- Product Code
- HTN
- 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 |
|---|---|---|---|
| HTN | Washer, Bolt Nut | FDA class 2 | Orthopedic |
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