FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
COAXIAL BONE AND VERTEBRAL BODY BIOPSY NEEDLE MODEL# JBC1213, JBC1208
K Number: K070091
·
Decision Apr 18, 2007
Classifications
1
FEI Numbers
207
Registration Numbers
207
Same Product Code
360
Applicant Total
26
Review Days
98
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Basic Information
- Device Name
- COAXIAL BONE AND VERTEBRAL BODY BIOPSY NEEDLE MODEL# JBC1213, JBC1208
- K Number
- K070091
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1075
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Cardinal Health, Inc.
- Date Received
- January 10, 2007
- Decision Date
- April 18, 2007
- Product Code
- KNW
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| KNW | Instrument, Biopsy | FDA class 2 | Gastroenterology, Urology |
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