Ascension Orthopedics, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Ascension Orthopedics, Inc. has 22 FDA 510(k) cleared orthopedic devices. Based in Austin, US.
Latest FDA clearance: May 2024. Active since 2002.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Ascension Orthopedics, Inc.
22 devices
Cleared
May 30, 2024
Freedom Wrist Arthroplasty System
Orthopedic
196d
Cleared
Dec 14, 2023
Ascension Silicone MCP
Orthopedic
29d
Cleared
Feb 13, 2013
INTEGRA PROXIMAL HUMERAL PLATE SYSTEM
Orthopedic
237d
Cleared
Dec 06, 2011
ASCENSION ATLAS HUMERAL PLATING SYSTEM
Orthopedic
267d
Cleared
Dec 21, 2010
THE ASCENSION MOVEMENT GREAT TOE SYSTEM TOTAL ARTHROPLASTY
Orthopedic
105d
Cleared
Aug 30, 2010
ASCENSION MODULAR TOTAL SHOULDER SYSTEM
Orthopedic
194d
Cleared
Aug 02, 2010
ASCENSION TOTAL PLATE SYSTEM
Orthopedic
161d
Cleared
Jul 12, 2010
ASCENSION ANKLE FUSION NAIL SYSTEM
Orthopedic
101d
Cleared
Jun 16, 2010
ASCENSION ANKLE FUSION PLATE SYSTEM
Orthopedic
146d
Cleared
Jan 14, 2010
ASCENSION METAL GREAT TOE SYSTEM
Orthopedic
192d
Cleared
Nov 05, 2009
ASCENSION CANNULATED SCREW SYSTEM
Orthopedic
87d
Cleared
Jan 12, 2009
ASCENSION SILICONE PIP
Orthopedic
158d