Medical Device Manufacturer · US , Lancaster , PA

Keos - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2016
Official Website
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Keos Orthopedic ✕
4 devices
1-4 of 4
Cleared Jun 06, 2022
Keos Anterior Cervical Interbody Fusion Device System
K212450 · ODP
Orthopedic · 305d
Cleared Dec 16, 2019
Keos Lumbar IBFD
K193174 · MAX
Orthopedic · 28d
Cleared Apr 10, 2017
Keos Lumbar IBFD
K163386 · MAX
Orthopedic · 129d
Cleared Jul 15, 2016
Keos Lumbar IBFD
K160631 · MAX
Orthopedic · 130d
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