Ascension Orthopedic is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ascension Orthopedic - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Ascension Orthopedic has 7 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 7 cleared submissions from 2011 to 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ascension Orthopedic Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ascension Orthopedic
7 devices
Cleared
Oct 10, 2014
INTEGRA EXTERNAL FIXATION SYSTEM
Orthopedic
228d
Cleared
Aug 07, 2013
INTEGRA TITANIUM BONE WEDGE
Orthopedic
86d
Cleared
Jun 18, 2013
TITAN REVERSE SHOULDER SYSTEM
Orthopedic
160d
Cleared
Apr 11, 2012
TITAN MODULAR TOTAL SHOULDER SYSTEM
Orthopedic
231d
Cleared
Apr 09, 2012
FIRST CHOICE DRUJ SYSTEM, PARTIAL HEAD IMPLANT
Orthopedic
224d
Cleared
Nov 04, 2011
ASCENSION NUGRIP CMC IMPLANT
Orthopedic
87d
Cleared
Aug 19, 2011
NUGAIT(TM) SUBTALAR IMPLANT SYSTEM
Orthopedic
53d