FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DEPUY SUMMIT BASIC PRESS-FIT HIP STEM
K Number: K030122
·
Decision Feb 5, 2003
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
80
Applicant Total
207
Review Days
22
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Basic Information
- Device Name
- DEPUY SUMMIT BASIC PRESS-FIT HIP STEM
- K Number
- K030122
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3360
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- DePuy Orthopaedics, Inc.
- Date Received
- January 14, 2003
- Decision Date
- February 5, 2003
- Product Code
- LWJ
- 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 |
|---|---|---|---|
| LWJ | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented | FDA class 2 | Orthopedic |
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