MagnetOs Easypack Putty
K-Number: K233607 · 2023-12-15
ApplicantKuros Biosciences B.V
Decision Date2023-12-15
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MagnetOs Easypack Putty is a medical device manufactured by Kuros Biosciences B.V. It received FDA 510(k) clearance on 2023-12-15 under approval number K233607. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MagnetOs Easypack Putty?
MagnetOs Easypack Putty is a medical device that received FDA 510(k) clearance on 2023-12-15. It is manufactured by Kuros Biosciences B.V. The 510(k) number is K233607.
When was MagnetOs Easypack Putty approved by the FDA?
MagnetOs Easypack Putty received FDA 510(k) clearance on 2023-12-15, under approval number K233607.
What company makes MagnetOs Easypack Putty?
MagnetOs Easypack Putty is manufactured by Kuros Biosciences B.V.
What is the FDA product code for MagnetOs Easypack Putty?
The FDA product code for MagnetOs Easypack Putty is MQV.
Related Clinical Trials
NCT07225751
A Prospective, Randomized, Single-blind, Controlled, Multi-center Study to Assess the Safety and Performance of MagnetOsTM Compared to Autogenous Bone Graft in Patients Undergoing Hindfoot or Ankle Fusions.
RECRUITING
NCT07512336
A Randomized Intra-Patient Controlled Trial of MagnetOs™ Putty vs Autograft in Instrumented Posterolateral Spinal Fusion in Idiopathic Scoliosis Patients
NOT_YET_RECRUITING
Other Devices by Kuros Biosciences B.V
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.