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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