Metasurg - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Metasurg has 5 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 5 cleared submissions from 2007 to 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Metasurg Filter by specialty or product code using the sidebar.
5 devices
Cleared
May 03, 2013
METASURG NITINOL STAPLE IMPLANT
Orthopedic
134d
Cleared
Aug 09, 2011
METASURG SUBTALAR IMPLANT
Orthopedic
97d
Cleared
Jul 21, 2011
METASURG DIGIFUSE IMPLANT
Orthopedic
49d
Cleared
Feb 13, 2009
METASURG CANNULATED TIATANIUM HEMI IMPLANT, MODEL HM-1000
Orthopedic
81d
Cleared
May 08, 2007
METASURG SUBTALAR IMPLANT
Orthopedic
82d