FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DISTAL CENTRALIZER, EXETER II HIP SYSTEM
K Number: K974054
·
Decision Dec 23, 1997
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
560
Applicant Total
36
Review Days
57
Basic Information
- Device Name
- DISTAL CENTRALIZER, EXETER II HIP SYSTEM
- K Number
- K974054
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3350
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- HOWMEDICA, INC.
- Date Received
- October 27, 1997
- Decision Date
- December 23, 1997
- 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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