FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇪 Ireland
DEPUY ATTUNE KNEE SYSTEM - CEMENTLESS CR AND PS FEMORAL COMPONENETS
K Number: K140881
·
Decision Feb 13, 2015
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
142
Applicant Total
13
Review Days
312
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Basic Information
- Device Name
- DEPUY ATTUNE KNEE SYSTEM - CEMENTLESS CR AND PS FEMORAL COMPONENETS
- K Number
- K140881
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3565
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Depuy(Ireland)
- Date Received
- April 7, 2014
- Decision Date
- February 13, 2015
- Product Code
- MBH
- 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 |
|---|---|---|---|
| MBH | Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer | FDA class 2 | Orthopedic |
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| K170806 | ATTUNE Cemented Tibial Base, Fixed Bearing | Jun 15, 2017 | Substantially Equivalent |
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