FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FORCEPS
K Number: K771746
·
Decision Sep 26, 1977
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
303
Review Days
11
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Basic Information
- Device Name
- FORCEPS
- K Number
- K771746
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Depuy, Inc.
- Date Received
- September 15, 1977
- Decision Date
- September 26, 1977
- Product Code
- GEN
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| GEN | Forceps, General & Plastic Surgery | FDA class 1 | General, Plastic Surgery |
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| K020541 | AGILITY ANKLE REVISION PROSTHESIS | May 20, 2002 | Substantially Equivalent |
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