Osteosymbionics, LLC is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osteosymbionics, LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Osteosymbionics, LLC has 4 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Historical record: 4 cleared submissions from 2007 to 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Osteosymbionics, LLC Filter by specialty or product code using the sidebar.
Osteosymbionics, LLC — FDA 510(k) Products and Clearance History
4 devices
Cleared
May 20, 2014
OSTEOSYMBIONICS PATIENT-SPECIFIC CRANIAL PLATE
Neurology
232d
Cleared
Aug 08, 2012
OSTEOSYMBIONICS PEEK CRANIAL IMPLANT
Neurology
119d
Cleared
Sep 22, 2011
OSTEOSYMBIONICS, ST TEMPORALIS IMPLANT
General & Plastic Surgery
157d
Cleared
Dec 10, 2007
OSTEOSYMBIONICS PATIENT SPECIFIC CRANIAL IMPLANT
Neurology
87d