FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BIOMET CALCANEAL PLATE
K Number: K022515
·
Decision Sep 17, 2002
Classifications
1
FEI Numbers
505
Registration Numbers
505
Same Product Code
1254
Applicant Total
34
Review Days
49
Basic Information
- Device Name
- BIOMET CALCANEAL PLATE
- K Number
- K022515
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- BIOMET ORTHOPEDICS, INC.
- Date Received
- July 30, 2002
- Decision Date
- September 17, 2002
- Product Code
- HRS
- 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 |
|---|---|---|---|
| HRS | Plate, Fixation, Bone | FDA class 2 | Orthopedic |
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