Scandius Biomedical, Inc.
Scandius Biomedical, Inc. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2006.
Top product codes for Scandius Biomedical, Inc.
Recent clearances by Scandius Biomedical, Inc.
- K063497 — MODIFICATION TO SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM
- K063499 — MODIFICATION TO SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM
- K060522 — SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM
- K052810 — SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM
- K041961 — SCANDIUS ABSORBABLE ACL RECONSTRUCTION SYSTEM
- K041749 — SCANDIUS ACL RECONSTRUCTION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.