FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ARTHROCARE PERCD SPINEWAND
K Number: K030954
·
Decision Apr 16, 2003
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
112
Review Days
20
Basic Information
- Device Name
- ARTHROCARE PERCD SPINEWAND
- K Number
- K030954
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 878.4400
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- ARTHROCARE CORP.
- Date Received
- March 27, 2003
- Decision Date
- April 16, 2003
- Product Code
- GEI
- 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 |
|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | FDA class 2 | General, Plastic Surgery |
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| K111397 | TITAN TI SUTURE ANCHOR SYSTEM | Jul 12, 2011 | Substantially Equivalent |
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