FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120
K Number: K021760
·
Decision Aug 27, 2002
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
14
Review Days
90
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Basic Information
- Device Name
- NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120
- K Number
- K021760
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.4560
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Orthosoft, Inc.
- Date Received
- May 29, 2002
- Decision Date
- August 27, 2002
- 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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