FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ARTHREX BIOWIRE
K Number: K091018
·
Decision Jul 30, 2010
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
16
Applicant Total
348
Review Days
477
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Basic Information
- Device Name
- ARTHREX BIOWIRE
- K Number
- K091018
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.5000
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Arthrex, Inc.
- Date Received
- April 9, 2009
- Decision Date
- July 30, 2010
- Product Code
- GAS
- 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 |
|---|---|---|---|
| GAS | Suture, Nonabsorbable, Synthetic, Polyester | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Arthrex, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K253931 | Arthrex Bioabsorbable PushLock Suture Anchors | May 28, 2026 | Substantially Equivalent |
| K254215 | Arthrex Beaming System | May 8, 2026 | Substantially Equivalent |
| K252016 | Arthrex Humeral Nails | Mar 20, 2026 | Substantially Equivalent |
| K260561 | Arthrex FiberTak Suture Anchor | Mar 20, 2026 | Substantially Equivalent |
| K260405 | FiberTape Button | Mar 9, 2026 | Substantially Equivalent |
| K252196 | Arthrex FibuLock Nail System | Mar 5, 2026 | Substantially Equivalent |
| K260353 | Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button | Mar 3, 2026 | Substantially Equivalent |
| K254229 | Arthrex Nano FiberTak Suture Anchor | Mar 2, 2026 | Substantially Equivalent |
| K253713 | Arthrex Variable Angle (VA) Proximal Tibia Plating System | Jan 21, 2026 | Substantially Equivalent |
| K252807 | Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates | Jan 12, 2026 | Substantially Equivalent |