Sulzermedica - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Sulzermedica has 5 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 5 cleared submissions from 1999 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sulzermedica Filter by specialty or product code using the sidebar.
5 devices
Cleared
Aug 24, 2000
MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA
Orthopedic
24d
Cleared
Jan 28, 2000
SULZER VASCUTEK SEALPTFE VASCULAR PROSTHESIS
Cardiovascular
88d
Cleared
Dec 09, 1999
SULZER VASCUTEK GELSOFT VASCULAR PROSTHESIS
Cardiovascular
295d
Cleared
Dec 01, 1999
APR METASUL ACETABULAR INSERT
Orthopedic
41d
Cleared
Nov 19, 1999
SULZER VASCUTEK EPTFE VASCULAR PROSTHESIS
Cardiovascular
88d