FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
ZIMMER ANATOMIC HIP SYSTEM
K Number: K922071
·
Decision Feb 22, 1994
Classifications
1
FEI Numbers
271
Registration Numbers
271
Same Product Code
551
Applicant Total
308
Review Days
659
Basic Information
- Device Name
- ZIMMER ANATOMIC HIP SYSTEM
- K Number
- K922071
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3358
- Medical Specialty
- Orthopedic
- Decision
- Unknown
- Statement or Summary
- Statement
- Applicant
- ZIMMER, INC.
- Date Received
- May 4, 1992
- Decision Date
- February 22, 1994
- Product Code
- LPH
- 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 |
|---|---|---|---|
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | FDA class 2 | Orthopedic |
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