510(k) K231556

Device
SPECTRUM® GV Bone Cement
Applicant
Osteoremedies, LLC
510(k) number
K231556
Product code
LOD
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-20
Date received
2023-05-30
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
Eric Stookey
Address
6800 Poplar Ave. Suite 120 Memphis TN US 38138 38138

FDA Registration Numbers

Source Documents

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

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K210125BonOs HV Genta, BonOs MV Genta, BonOs LV GentaOsartis GmbH2021-03-19
K210120BonOs HV, BonOs MV, BonOs LVOsartis GmbH2021-03-19
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K193059G1 40 Radiopaque Bone CementG21, S.R.L.2020-03-19
K193061G3 40 Radiopaque Bone CementG21, S.R.L.2020-03-19
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