510(k) K254107

Device
Refobacin Bone Cement R (110034355)
Applicant
Biomet France
510(k) number
K254107
Product code
LOD
Decision
Substantially Equivalent (SESE)
Decision date
2026-04-15
Date received
2025-12-19
Regulation
888.3027
Classification name
Bone Cement
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Vanessa Gautier
Address
Plateau De Lautagne Valence FR 26000 26000

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code LOD

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K250760SPECTRUM GV Bone CementOsteoremedies, LLC2025-04-02
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K231556SPECTRUM® GV Bone CementOsteoremedies, LLC2023-12-20
K211163Bone Cement Genta, Bone Cement HV, Bone Cement LVTecres S.P.A.2023-01-09
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K213812PALACOS MV proHeraeus Medical GmbH2022-02-02
K210607PALACOS R pro, PALACOS R+G pro, PALACOS MV+G proHeraeus Medical GmbH2021-07-09
K202458BonOs Inject, Pedicle screw kits, Cement pusherOsartis GmbH2021-05-18
K210125BonOs HV Genta, BonOs MV Genta, BonOs LV GentaOsartis GmbH2021-03-19
K210120BonOs HV, BonOs MV, BonOs LVOsartis GmbH2021-03-19
K202475PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+GHeraeus Medical GmbH2020-11-23
K193059G1 40 Radiopaque Bone CementG21, S.R.L.2020-03-19
K193061G3 40 Radiopaque Bone CementG21, S.R.L.2020-03-19
K192394Hi-Fatigue Bone CementOsartis GmbH2019-12-02