Osseus Fusion Systems, LLC

5 FDA 510(k) medical device clearances.

Top product codes for Osseus Fusion Systems, LLC

Recent clearances by Osseus Fusion Systems, LLC

K213590 — Blue Topaz Sacroiliac Screw System OUR · 2022-03-01
K181347 — Aries® Lumbar Interbodies MAX · 2018-08-15
K170844 — Gemini-C Hybrid Cervical Interbody System ODP · 2017-07-03
K160522 — White Pearl Preferred Angle Anterior Cervical Plate KWQ · 2016-04-26
K131810 — OSSEUS BLACK DIAMOND PEDICLE SCREW SYSTEM MNH · 2013-08-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.