Isotis NV - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Isotis NV has 8 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 8 cleared submissions from 2000 to 2007. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Isotis NV Filter by specialty or product code using the sidebar.
8 devices
Cleared
Aug 15, 2007
ACCELI DBM FAMILY PRODUCTS, 0.5CC, 1CC, 2.5CC, 5CC, 10CC, 15CC, 30CC
Orthopedic
408d
Cleared
Mar 29, 2006
ORTHOBLAST II DBM DEMINERALIZED BONE MATRIX PASTE AND PUTTY
Dental
48d
Cleared
Mar 27, 2006
ACCELL CONNEXUS DEMINERALIZED BONE MATRIX PUTTY
Dental
48d
Cleared
Aug 20, 2004
OSSATURA DENTAL
Dental
435d
Cleared
Jul 16, 2004
OPEN BORE SYRINGE
General Hospital
57d
Cleared
May 20, 2003
OSSATURA BCP BONE VOID FILLER
Orthopedic
126d
Cleared
Apr 20, 2001
SYNPLUG
Orthopedic
30d
Cleared
May 04, 2000
SHUTTLE STOP
Orthopedic
72d