ClearanceBrief
Company ยท NL

Kuros Biosciences B.V

FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2025. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MQVFiller, Bone Void, Calcium Compound12
MAXIntervertebral Fusion Device With Bone Graft, Lumbar1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 23, 2025K243474MagnetOs MIS
Kuros Biosciences B.V, NL
MQV
Jun 27, 2024K241212MagnetOs Easypack Putty
Kuros Biosciences, NL
MQV
Apr 1, 2024K240442MagnetOs Putty
Kuros Biosciences B.V, NL
MQV
Jan 19, 2024K232347MagnetOs Granules
Kuros Biosciences B.V, NL
MQV
Dec 20, 2023K230736MagnetOs Putty
Kuros Biosciences B.V, NL
MQV
Dec 15, 2023K233607MagnetOs Easypack Putty
Kuros Biosciences B.V, NL
MQV
Nov 21, 2023K233245MagnetOs Flex Matrix
Kuros Biosciences B.V, NL
MQV
Apr 14, 2022K213959MagnetOs Flex Matrix
Kuros Biosciences B.V, NL
MQV
Jan 10, 2022K213111MagnetOs granules
Kuros Biosciences B.V, NL
MQV
Sep 2, 2021K211201MagnetOs Easypack Putty
Kuros Biosciences B.V, NL
MQV
Mar 8, 2019K183092Kuros TLIF Cage
Kuros Biosciences B.V, NL
MAX
Dec 6, 2018K181958MagnetOs Putty
Kuros Biosciences B.V, NL
MQV
Aug 24, 2017K171563MagnetOs Putty
Kuros Biosciences B.V, NL
MQV

Latest recalls

DateFirm and productCodeLinked 510(k)
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