FDA 510(k) Applications Submitted by KRISTI KISTNER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K050416 |
02/18/2005 |
OSSAPLAST ORTHO |
OSSACUR AG |
| K051047 |
04/25/2005 |
COLLOSS E BONE VOID FILLER |
OSSACUR AG |
| K042305 |
08/25/2004 |
OSSAPLAST ORTHO, O.5ML, MODEL# 221 900, OSSAPLAST ORTHO, 1.0ML, MODEL# 221 901, OSSAPLAST ORTHO, 3.0ML, MODEL# 221 903 |
OSSACUR AG |
| K053374 |
12/05/2005 |
OSSAPLAST DENTAL (PARTICLE SIZE OF 500 TO 1000 UM TO 2000 UM) |
OSSACUR AG |
| K083701 |
12/15/2008 |
PANASIL INITIAL CONTACT AND PANASIL TRAY |
KETTENBACH GMBH & CO KG |
| K981076 |
03/24/1998 |
VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT |
IMPRA, INC. |
| K981079 |
03/24/1998 |
VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT |
IMPRA, INC. |
| K991027 |
03/29/1999 |
BI-DIRECTIONAL TUNNELER |
IMPRA, INC. |
| K971192 |
03/31/1997 |
IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT |
IMPRA, INC. |
| K983064 |
09/02/1998 |
IMPRA HIGH POROSITY GRAFT |
IMPRA, INC. |
| K983769 |
10/26/1998 |
DISTAFLO BYPASS GRAFT |
IMPRA, INC. |
| K983861 |
11/02/1998 |
DISTAFLO BYPASS GRAFT |
IMPRA, INC. |
| K964877 |
12/05/1996 |
IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT |
IMPRA, INC. |
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