FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
WORRELL TRIAL PATELLA
K Number: K771709
·
Decision Oct 6, 1977
Classifications
1
FEI Numbers
434
Registration Numbers
434
Same Product Code
9
Applicant Total
303
Review Days
24
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Basic Information
- Device Name
- WORRELL TRIAL PATELLA
- K Number
- K771709
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 888.4800
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- Depuy, Inc.
- Date Received
- September 12, 1977
- Decision Date
- October 6, 1977
- Product Code
- HWT
- 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 |
|---|---|---|---|
| HWT | Template | FDA class 1 | Orthopedic |
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