FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DePuy Synthes 3.5/4.5 mm Variable Angle LCP Periprosthetic Proximal Femur Plating System
K Number: K210205
·
Decision Mar 26, 2021
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
45
Review Days
59
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Basic Information
- Device Name
- DePuy Synthes 3.5/4.5 mm Variable Angle LCP Periprosthetic Proximal Femur Plating System
- K Number
- K210205
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Synthes (USA) Products, LLC
- Date Received
- January 26, 2021
- Decision Date
- March 26, 2021
- 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 |
Similar 510(k) Clearances
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|---|---|---|---|
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| K201336 | DePuy Synthes Tibial Nail Advanced, Depuy Synthes Locking Screws Medullary Nails, 4.0 and 5.0mm | Sep 3, 2020 | Substantially Equivalent |
| K191463 | DePuy Synthes Hammertoe Continuous Compression Implant | Feb 26, 2020 | Substantially Equivalent |