FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STEINMAN PIN
K Number: K960483
·
Decision Apr 9, 1996
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
4
Review Days
67
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Basic Information
- Device Name
- STEINMAN PIN
- K Number
- K960483
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- American Medical Specialties, Inc.
- Date Received
- February 2, 1996
- Decision Date
- April 9, 1996
- Product Code
- HTY
- 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 |
|---|---|---|---|
| HTY | Pin, Fixation, Smooth | FDA class 2 | Orthopedic |
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