FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
3M HS 22 FEMORAL COMPONENT
K Number: K792181
·
Decision Nov 15, 1979
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
106
Applicant Total
331
Review Days
17
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Basic Information
- Device Name
- 3M HS 22 FEMORAL COMPONENT
- K Number
- K792181
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3360
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- 3M Company
- Date Received
- October 29, 1979
- Decision Date
- November 15, 1979
- Product Code
- KWL
- 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 |
|---|---|---|---|
| KWL | Prosthesis, Hip, Hemi-, Femoral, Metal | FDA class 2 | Orthopedic |
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