EPORE® XO cup system
FDA 510(k) K252451 · Implantcast GmbH
Submission
- Device name
- EPORE® XO cup system
- Applicant
- Implantcast GmbH
Buxtehude, DE - Received
- August 4, 2025
- Decision date
- April 24, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- OQI – Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3353
- Specialty
- Orthopedic
- Implant
- Yes
1. Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis. 2. Rheumatoid arthritis. 3. Correction of functional deformity. 4. Treatment of non-union, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable by other techniques. 5. Revision procedures where other treatment or devices have failed. Cemented and…
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Questions and answers
When was EPORE® XO cup system cleared by the FDA?
EPORE® XO cup system (K252451) received a 510(k) decision of Substantially Equivalent on April 24, 2026, 263 days after the submission was received.
What is the product code of K252451?
The FDA product code is OQI – Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented, a Class II (moderate risk) device regulated under 21 CFR 888.3353.