Scandius Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Scandius Biomedical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Scandius Biomedical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 6 cleared submissions from 2004 to 2006. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Scandius Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scandius Biomedical, Inc.
6 devices
Cleared
Dec 19, 2006
MODIFICATION TO SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM
Orthopedic
29d
Cleared
Dec 19, 2006
MODIFICATION TO SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM
Orthopedic
29d
Cleared
Apr 11, 2006
SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM
Orthopedic
43d
Cleared
Dec 20, 2005
SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM
Orthopedic
77d
Cleared
Oct 20, 2004
SCANDIUS ABSORBABLE ACL RECONSTRUCTION SYSTEM
Orthopedic
91d
Cleared
Sep 08, 2004
SCANDIUS ACL RECONSTRUCTION SYSTEM
Orthopedic
71d