FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

MagnetOs Putty

K Number: K230736 · Decision Dec 20, 2023
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
12
Review Days
278

Basic Information

Device Name
MagnetOs Putty
K Number
K230736
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kuros Biosciences B.V
Date Received
March 17, 2023
Decision Date
December 20, 2023
Product Code
MQV
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
MQV Filler, Bone Void, Calcium Compound

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQV), ordered by most recent decision date.

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Other Clearances by Kuros Biosciences B.V

K Number Device Name
K243474 MagnetOs MIS
K240442 MagnetOs Putty
K232347 MagnetOs Granules
K233607 MagnetOs Easypack Putty
K233245 MagnetOs Flex Matrix
K213959 MagnetOs Flex Matrix
K213111 MagnetOs granules
K211201 MagnetOs Easypack Putty
K183092 Kuros TLIF Cage
K181958 MagnetOs Putty
Search all 12 clearances from Kuros Biosciences B.V →