FDA 510(k) Applications Submitted by VICTORIA MACKINNON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K970285 |
01/24/1997 |
AESUCLAP SOCON SPINAL SYSTEM |
AESCULAP, INC. |
| K960470 |
02/01/1996 |
NEURO-PATCH |
AESCULAP, INC. |
| K970549 |
02/12/1997 |
TITANIUM ALLOY BONE SCREWS |
AESCULAP, INC. |
| K970851 |
03/07/1997 |
LYOPLANT DURA SUBSTITUTE(VARIOUS) |
AESCULAP, INC. |
| K122003 |
07/09/2012 |
RENEW INSERT |
RENEW MEDICAL, INC. |
| K062028 |
07/18/2006 |
CYSTIC FIBROSIS GENOTYPING ASSAY, MODEL 6L20-01 |
CELERA DIAGNOSTICS |
| K954394 |
09/18/1995 |
AESCULAP VENTRICULOSCOPE SYSTEM |
AESCULAP, INC. |
| K983758 |
10/26/1998 |
YASARGIL TITANIUM ANEURYSM CLIPS |
AESCULAP, INC. |
| K970050 |
01/06/1997 |
YASARGIL TITANIUM ANEURYSM CLIPS (FTXXXT) |
AESCULAP, INC. |
| K111804 |
06/27/2011 |
INTELLISPACE PACS 4.X |
PHILIPS HEALTHCARE INFORMATICS, INC. |
|
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