FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ARTHREX FIBERWIRE
K Number: K071622
·
Decision Jul 3, 2007
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
348
Review Days
19
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Basic Information
- Device Name
- ARTHREX FIBERWIRE
- K Number
- K071622
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 878.5000
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Arthrex, Inc.
- Date Received
- June 14, 2007
- Decision Date
- July 3, 2007
- Product Code
- GAT
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene | FDA class 2 | General, Plastic Surgery |
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