FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ORTHOPILOT
K Number: K003347
·
Decision Feb 23, 2001
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
33
Review Days
121
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Basic Information
- Device Name
- ORTHOPILOT
- K Number
- K003347
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.4560
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Kinamed, Inc.
- Date Received
- October 25, 2000
- Decision Date
- February 23, 2001
- Product Code
- HAW
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| HAW | Neurological Stereotaxic Instrument | FDA class 2 | Neurology |
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