FDA 510(k) Applications Submitted by SHARON MCDERMOTT
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K170170 |
01/19/2017 |
Valleylab FT10 Electrosurgical Platform |
Covidien llc |
K090348 |
02/11/2009 |
CODMAN BACTISEAL EVD CATHETER SET, CODMAN BACTISEAL CLEAR EVD CATHETER SET |
Codman & Shurtleff, Inc. |
K160539 |
02/26/2016 |
BiZact Open Sealer/Divider |
COVIDIEN |
K130608 |
03/07/2013 |
QUADCUT |
MEDTRONIC NAVIGATION, INC. |
K110751 |
03/18/2011 |
CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER |
Codman & Shurtleff, Inc. |
K171066 |
04/10/2017 |
BiZact Tonsillectomy Device Advanced Bipolar Tissue Sealer/Divider |
Covidien, llc |
K211269 |
04/27/2021 |
Visualase MRI-Guided Laser Ablation System (SW 3.4) |
Medtronic Navigation, Inc. |
K091346 |
05/07/2009 |
CODMAN HAKIM MICRO II VALVE |
Codman & Shurtleff, Inc. |
K041421 |
05/28/2004 |
NAME BONE VOID FILLER |
STRYKER BIOTECH |
K151649 |
06/18/2015 |
Valleylab FT10 Electrosurgical Platform |
COVIDIEN |
K102589 |
09/09/2010 |
CODMAN BACTISEAL CATHETERS, CODMAN BACTISEAL EVD CATHETER |
Codman & Shurtleff, Inc. |
K172757 |
09/13/2017 |
Valleylab FX8 Electrosurgical Platform |
Covidien llc |
K143161 |
11/03/2014 |
Force FX-8(S), Force FX-8C(S), Force FX-8CA(S) |
COVIDIEN |
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