FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Eminent Foot Plate System
K Number: K143365
·
Decision Mar 30, 2015
Classifications
1
FEI Numbers
505
Registration Numbers
505
Same Product Code
1254
Applicant Total
5
Review Days
126
Basic Information
- Device Name
- Eminent Foot Plate System
- K Number
- K143365
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Eminent Spine
- Date Received
- November 24, 2014
- Decision Date
- March 30, 2015
- 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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|---|---|---|---|
| K241663 | Eminent Spine 3D Titanium Pedicle Screw System | Apr 28, 2025 | Substantially Equivalent |
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| K212701 | Eminent Spine 3D Cervical Interbody Fusion System | Feb 6, 2023 | Substantially Equivalent |
| K221936 | Standalone ALIF Interbody Fusion System | Oct 17, 2022 | Substantially Equivalent |