FDA 510(k) Applications Submitted by JENNIFER BRENNAN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K120258 |
01/27/2012 |
DUET TRS RELOADS, DUET TRS RELOADS WITH TRI-STAPLE TECHNOLOGY, ENDO GIA UNIVERSAL AND ULTRA UNIVERSAL STAPLERS |
COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H |
| K100257 |
01/28/2010 |
VLOC9ABSORBABLE WOUND CLOSURE DEVICE |
SURGICAL DEVICES, A DIVISION OF TYCO HEALTHCARE |
| K090470 |
02/23/2009 |
AUTOSUTURE PROTACK; TACKER SYSTEM; ABSORBATACK FIXATION DEVICES |
COVIDIEN |
| K000691 |
02/29/2000 |
VULCAN ELECTROSURGICAL PROBES: VULCAN MICRO LIGAMENT CHISELS, VULCAN LIGAMENT CHISELS, VULCAN EFLEX LIGAMENT CHISELS |
ORATEC INTERVENTIONS, INC. |
| K091087 |
04/15/2009 |
MODIFICATION TO V-LOC 180 ABSORBABLE WOUND CLOSURE DEVICE |
SURGICAL DEVICES, TYCO HEALTHCARE GROUP LP |
| K071406 |
05/21/2007 |
AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER |
UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC |
| K142091 |
08/01/2014 |
PARIETENE MACROPOROUS MESH |
SOFRADIM PRODUCTION |
| K992805 |
08/20/1999 |
ORATEC ABLATOR-S PROBES (MONOPOLAR ABLATION SUCTION PROBES) |
ORATEC INTERVENTIONS, INC. |
| K103052 |
10/14/2010 |
V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE |
Covidien LLC |
| K993967 |
11/23/1999 |
ORATEC SPINECATH INTRADISCAL CATHETER, MODEL 920002 |
ORATEC INTERVENTIONS, INC. |
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