Medical Device Manufacturer · US , North Attleboro , MA

Isotis NV - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2000
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
1–8 of 8
ACCELI DBM FAMILY PRODUCTS, 0.5CC, 1CC, 2.5CC, 5CC, 10CC, 15CC, 30CC
K061880 · MQV Filler, Bone Void, Calcium Compound · Orthopedic
Aug 2007 408d
ORTHOBLAST II DBM DEMINERALIZED BONE MATRIX PASTE AND PUTTY
K060332 · NUN Bone Grafting Material, Human Source · Dental
Mar 2006 48d
ACCELL CONNEXUS DEMINERALIZED BONE MATRIX PUTTY
K060306 · NUN Bone Grafting Material, Human Source · Dental
Mar 2006 48d
OSSATURA DENTAL
K031813 · LYC Bone Grafting Material, Synthetic · Dental
Aug 2004 435d
OPEN BORE SYRINGE
K041344 · FMF Syringe, Piston · General Hospital
Jul 2004 57d
OSSATURA BCP BONE VOID FILLER
K030131 · MQV Filler, Bone Void, Calcium Compound · Orthopedic
May 2003 126d
SYNPLUG
K010840 · LZN Cement Obturator · Orthopedic
Apr 2001 30d
SHUTTLE STOP
K000587 · LZN Cement Obturator · Orthopedic
May 2000 72d
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All8 Orthopedic 4 Dental 3 General Hospital 1