EPORE® XO cup system
FDA 510(k) clearance K252451 · decided 2026-04-24
Clearance details
- K-number
- K252451
- Device name
- EPORE® XO cup system
- Applicant
- Implantcast GmbH
- Decision
- Substantially Equivalent
- Date received
- 2025-08-04
- Decision date
- 2026-04-24
- Days to decision
- 263 days
- Clearance type
- Traditional
- Product code
- OQI
- Device class
- 2
- Regulation number
- 888.3353
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Buxtehude, DE
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Libertas E-XLPE Modular Liner (K192989) | Maxx Orthopedics, Inc. | 2020-10-29 |
| E-XPE Acetabular Components and U-Motion II Acetabular Cup (K172833) | United Orthopedic Corporation | 2018-06-12 |
| Exactech® Novation® and AcuMatch® E-HXL Acetabular Liners (K173583) | Exactech, Inc. | 2018-03-12 |
| CORIN TRINITY ACETABULAR SYSTEM ECIMA LINERS (K111481) | Corin USA | 2012-02-06 |
Recalls involving this device
No recalls on record reference this clearance.