FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
EPORE® XO cup system
K Number: K252451
·
Decision Apr 24, 2026
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
4
Applicant Total
20
Review Days
263
Basic Information
- Device Name
- EPORE® XO cup system
- K Number
- K252451
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3353
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Implantcast GmbH
- Date Received
- August 4, 2025
- Decision Date
- April 24, 2026
- Product Code
- OQI
- 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 |
|---|---|---|---|
| OQI | Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented | FDA class 2 | Orthopedic |
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Other Clearances by Implantcast GmbH
| K Number | Device Name | ||
|---|---|---|---|
| K260037 | implantcast Packaging System Update | Mar 30, 2026 | Substantially Equivalent |
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| K241944 | AGILON® XO Shoulder Replacement System | Mar 10, 2025 | Substantially Equivalent |
| K240391 | MUTARS® femoral stem cemented 160 mm and 200 mm | Oct 24, 2024 | Substantially Equivalent |
| K234044 | ACS® LD FB Knee System | Sep 6, 2024 | Substantially Equivalent |
| K240834 | EcoFit® short stem cementless cpTi | Jun 3, 2024 | Substantially Equivalent |
| K231657 | AGILON® XO Shoulder Replacement System | Feb 16, 2024 | Substantially Equivalent |
| K232371 | Actinia® hip stems | Oct 19, 2023 | Substantially Equivalent |
| K223103 | BethaLoc® stem cementless HA | Jun 20, 2023 | Substantially Equivalent |
| K222482 | AGILON XO Shoulder System | Sep 28, 2022 | Substantially Equivalent |