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
OQI Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented

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