FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ANATOMIC ADJUSTABLE AXIAL FIXATOR ASSEMBLY
K Number: K874377
·
Decision May 20, 1988
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
56
Applicant Total
1
Review Days
207
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Basic Information
- Device Name
- ANATOMIC ADJUSTABLE AXIAL FIXATOR ASSEMBLY
- K Number
- K874377
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- Harrington Arthritis Research Center
- Date Received
- October 26, 1987
- Decision Date
- May 20, 1988
- Product Code
- LXT
- 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 |
|---|---|---|---|
| LXT | Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite | FDA class 2 | Orthopedic |
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