Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by Osseus Fusion Systems, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K131810
06/19/2013
OSSEUS BLACK DIAMOND PEDICLE SCREW SYSTEM
OSSEUS FUSION SYSTEMS, LLC
K213590
11/12/2021
Blue Topaz Sacroiliac Screw System
Osseus Fusion Systems, LLC
K160522
02/25/2016
White Pearl Preferred Angle Anterior Cervical Plate
OSSEUS FUSION SYSTEMS, LLC
K170844
03/21/2017
Gemini-C Hybrid Cervical Interbody System
Osseus Fusion Systems, LLC
K181347
05/21/2018
Aries« Lumbar Interbodies
Osseus Fusion Systems, LLC
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact