FDA 510(k) Applications Submitted by ZHENG LIU
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K090124 |
01/21/2009 |
GRYPHON P BR DS ANCHOR W/ORTHOCORD,GRYPHON P BR ANCHOR W/ORTHOCORD, MODEL 210813,210814 |
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY |
K090669 |
03/13/2009 |
RIGIDFIX BIOCRYL CROSS PIN KITS |
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY |
K091041 |
04/13/2009 |
RIGIDFIX BIOCRYL 2.7MM BTB (210815), FEMORAL 3.3MM ST (210816), AND TIBIAL 3.3MM ST (210817) CROSS PIN KITS |
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY |
K111153 |
04/25/2011 |
SORBAFIX (TM) ABSORBABLE FIXATION SYSTEM, PERMAFIX (TM) FIXATION SYSTEM |
C.R. BARD, INC. |
K082643 |
09/11/2008 |
3.5 MM SIDE EFFECT ELECTRODE WITH INTEGRATED HANDPIECE, MODEL 227301, 3.5 MM ANGLED SIDE EFFECT ELECTRODE WITH INTEGRATE |
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY |
K092836 |
09/15/2009 |
OMNISPAN MENISCAL REPAIR SYSTEM/0 DEGREE, MODEL 228140, RAPIDLOC A2 MENISCAL REPAIR SYSTEM/12 DEGREE, MODEL 228141 |
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY |
K193056 |
11/01/2019 |
Puritan Bennett 980 Series Ventilator System |
Covidien, LLC |
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