FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BIOPRO 32MM BALL
K Number: K872856
·
Decision Aug 17, 1987
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
41
Review Days
27
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Basic Information
- Device Name
- BIOPRO 32MM BALL
- K Number
- K872856
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3350
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- Biopro, Inc.
- Date Received
- July 21, 1987
- Decision Date
- August 17, 1987
- Product Code
- JDI
- 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 |
|---|---|---|---|
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | FDA class 2 | Orthopedic |
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