FDA 510(k) Applications Submitted by FLORIN TRUUVERT
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090168 |
01/23/2009 |
AZUR DETACTABLE 18, MODELS 45-480305, 45-480310, 45-480405, 44-480415 |
MICROVENTION, INC. |
| K030392 |
02/05/2003 |
SAPPHIRE DETACHABLE COIL SYSTEM |
MICRO THERAPEUTICS, INC. |
| K090357 |
02/12/2009 |
HYDROFRAME (HES) |
MICROVENTION, INC. |
| K050543 |
03/02/2005 |
NEXUS DETACHABLE COIL SYSTEM |
MICRO THERAPEUTICS, INC. |
| K060625 |
03/09/2006 |
NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR |
MICRO THERAPEUTICS, INC. |
| K040694 |
03/17/2004 |
MODIFICATION TO SAPPHIRE DETACHABLE COIL SYSTEM (TETRIS 3-D) |
MICRO THERAPEUTICS, INC. |
| K060747 |
03/20/2006 |
FX DETACHABLE COIL SYSTEM |
MICRO THERAPEUTICS, INC. |
| K011436 |
05/10/2001 |
MOBILE-PATIENT VIEWER |
DATA CRITICAL CORPORATION |
| K051425 |
06/01/2005 |
NEXUS DETACHABLE COIL SYSTEM, HELIX SUPER SOFT CSR |
MICRO THERAPEUTICS, INC. |
| K051560 |
06/13/2005 |
NEXUS DETACHABLE COIL, MULTI-DIAMETER CSR AND HELIX SUPER SOFT CSR |
MICRO THERAPEUTICS, INC. |
| K031852 |
06/16/2003 |
SAPPHIRE DETACHABLE FIBER COILS |
MICRO THERAPEUTICS, INC. |
| K041649 |
06/17/2004 |
SAPPHIRE NXT DETACHABLE COIL SYSTEM |
MICRO THERAPEUTICS, INC. |
| K082385 |
08/19/2008 |
CHAPERON GUIDING CATHETER |
MICROVENTION, INC. |
| K082461 |
08/27/2008 |
BARE PLATINUM FRAMING COIL, MODEL(S) 100408BPFC-V,100412BPFC-V,100515BPFC-V100518BPFC-V,100522BPFC-V,100618BPFC-V100622B |
MICROVENTION, INC. |
| K033372 |
10/22/2003 |
SAPPHIRE DETACHABLE FIBERED COIL SYSTEM, HELIX FIBERED, CYCLONE, MULTIPLE MODELS |
MICRO THERAPEUTICS, INC. |
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