FDA 510(k) Applications Submitted by JACK GRIFFIS

FDA 510(k) Number Submission Date Device Name Applicant
K210665 03/05/2021 Nerve Tape BioCircuit Technologies, Incorporated
K091202 04/24/2009 WEDGELOC 180X STANDARD SUTURE ANCHOR WITH OPTI FIBER SUTURES,MODEL 1000-01 TAB VARYING DIAMETERS, MEDSHAPE SOLUTIONS
K211501 05/14/2021 Advantage-C PEEK Cervical lnterbody Fusion Device lntelivation, LLC
K141290 05/19/2014 HELICAL RIDGE PEEK INTERFERENCE SCREW MEDSHAPE, INC
K181546 06/12/2018 Dillard Nasal Balloon Catheter Intuit Medical Products, LLC
K181781 07/03/2018 DynaClipTM Bone Staple MedShape, Inc.
K092914 09/22/2009 WEDGELOC 180X (STANDARD) AND (CORTICAL) SUTURE ANCHOR WITH OPTI-FIBER SUTURES MEDSHAPE SOLUTIONS
K193305 11/29/2019 DynaClip Bone Staple MedShape, Inc.
K153484 12/03/2015 Dillard Airway Dilatation System INTUIT MEDICAL PRODUCTS, LLC
K083792 12/19/2008 WEDGELOC SUTURE ANCHOR WITH OPTI-FIBER SUTURES, MODEL 1000-01-055 MEDSHAPE SOLUTIONS
K143738 12/30/2014 DSS Sinusplasty Balloon Catheter Intuit Medical Products, LLC
K123264 10/18/2012 DK-PTCA BALLOON CATHETER INTUIT MEDICAL, LLC
K123350 10/31/2012 ECLIPSE SOFT TISSUE FASTENER MEDSHAPE, INC
K111471 05/27/2011 EXOSHAPE (TM) INTERFERENCE FIXATION DEVICE MODEL 1100-00-XXXX (VARIES BY SIZE) MEDSHAPE SOLUTIONS, INC


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