FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
Biolox® Delta Revision heads
K Number: K243809
·
Decision Mar 4, 2025
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
4
Review Days
83
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Basic Information
- Device Name
- Biolox® Delta Revision heads
- K Number
- K243809
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3353
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Limacorporate
- Date Received
- December 11, 2024
- Decision Date
- March 4, 2025
- Product Code
- LZO
- 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 |
|---|---|---|---|
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | FDA class 2 | Orthopedic |
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