FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LACTOSORB MENISCAL SCREW
K Number: K002020
·
Decision Aug 25, 2000
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
32
Review Days
53
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Basic Information
- Device Name
- LACTOSORB MENISCAL SCREW
- K Number
- K002020
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Biomet Manufacturing, Inc.
- Date Received
- July 3, 2000
- Decision Date
- August 25, 2000
- Product Code
- MAI
- 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 |
|---|---|---|---|
| MAI | Fastener, Fixation, Biodegradable, Soft Tissue | FDA class 2 | Orthopedic |
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