FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AMT SPINAL SYSTEM
K Number: K002059
·
Decision Nov 13, 2000
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
2
Review Days
130
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Basic Information
- Device Name
- AMT SPINAL SYSTEM
- K Number
- K002059
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3050
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Micron Precision Engineering, Inc.
- Date Received
- July 6, 2000
- Decision Date
- November 13, 2000
- Product Code
- KWP
- 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 |
|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | FDA class 2 | Orthopedic |
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Other Clearances by Micron Precision Engineering, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K022768 | AMT POLYAXIAL PEDICLE SCREW | Nov 13, 2002 | Substantially Equivalent |