FDA 510(k) Applications Submitted by DIANA L MARTONE

FDA 510(k) Number Submission Date Device Name Applicant
K130343 02/11/2013 CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS CORIN U.S.A.
K131647 06/05/2013 TRINITY ACETABULAR SYSTEM CORIN USA
K122305 08/01/2012 CORIN TRINITY-I ACETABULAR SHELL CORIN USA
K123705 12/03/2012 TRINITY NON-OCCLUDED TITANIUM PLASMA SPRAYED (TPS) ACETABULAR SHELLS CORIN USA
K142761 09/25/2014 Corin TaperFit Hip Stem CORIN USA
K170501 02/21/2017 CrossFT Knotless Biocomposite Suture Anchor with Disposable Driver ConMed Corporation
K190516 03/04/2019 MicroLink All-Suture Button Fixation System (Radiolucent) CONMED Corporation
K190582 03/06/2019 MicroLink All-Suture Button Fixation System (Radiopaque) CONMED Corporation
K180763 03/23/2018 CuffLink Implant System Biocomposite CONMED Corporation
K181120 04/27/2018 2.8 mm/3.3 mm PopLok Suture Anchors ConMed Corporation
K171592 05/31/2017 CrossFTÖ Knotless Biocomposite Suture Anchor with Disposable Driver ConMed Corporation
K182439 09/07/2018 TruShot with Y-Knot Shallow All-Suture Anchor ConMed Corporation
K182446 09/07/2018 TruShot with Y-Knot All-Suture Anchor ConMed Corporation
K182621 09/24/2018 CrossFT Knotless Deep Thread Suture Anchor with Disposable Driver ConMed Corporation
K152903 10/01/2015 REVIVAL(TM) Modular Revision Hip Stem CORIN USA
K153725 12/28/2015 Corin TaperFit Hip Stem CORIN USA LIMITED
K153772 12/31/2015 Corin TriFit TS Hip CORIN USA LIMITED


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