FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
EXTERNAL FIXATION SYSTEMS
K Number: K031181
·
Decision Jul 14, 2003
Classifications
1
FEI Numbers
247
Registration Numbers
247
Same Product Code
392
Applicant Total
423
Review Days
90
Basic Information
- Device Name
- EXTERNAL FIXATION SYSTEMS
- K Number
- K031181
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- SMITH & NEPHEW, INC.
- Date Received
- April 15, 2003
- Decision Date
- July 14, 2003
- Product Code
- KTT
- 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 |
|---|---|---|---|
| KTT | Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component | FDA class 2 | Orthopedic |
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