Medical Device Manufacturer · US , Broomfield , CO

Biomet Spine, LLC - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014
4
Total
4
Cleared
0
Denied

Biomet Spine, LLC has 4 FDA 510(k) cleared medical devices. Based in Broomfield, US.

Historical record: 4 cleared submissions from 2014 to 2016. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Biomet Spine, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Biomet Spine, LLC
4 devices
1-4 of 4
Cleared Jan 21, 2016
Biomet Spine Fusion System
K153695 · MAX
Orthopedic · 29d
Cleared Jul 31, 2015
Biomet Spine Fusion System
K151483 · MAX
Orthopedic · 59d
Cleared Mar 12, 2015
Biomet Spine Fusion System
K142634 · MAX
Orthopedic · 176d
Cleared Sep 25, 2014
POLARIS SPINAL SYSTEM - HA COATED
K141804 · NKB
Orthopedic · 84d
Filters
Filter by Specialty
All4 Orthopedic 4