FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TITAN TOTAL HIP DEVICE
K Number: K905298
·
Decision Jun 17, 1991
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
1
Review Days
202
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Basic Information
- Device Name
- TITAN TOTAL HIP DEVICE
- K Number
- K905298
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3350
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- Dr. Jean-Marc Guichet
- Date Received
- November 27, 1990
- Decision Date
- June 17, 1991
- 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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