Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

JDG 2018-03-19

Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads

Applicant Stryker Orthopaedics

K-Number K173499

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LOX 2018-03-19

OTW Takeru PTCA Balloon Dilatation Catheter

Applicant KANEKA Corporation

K-Number K172264

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JEC 2018-03-19

Anjon Bremer Halo System

Applicant Anjon Holdings, LLC

K-Number K171863

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GCJ 2018-03-19

Ezee Retrieval

Applicant Genicon, Inc.

K-Number K180579

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DQX 2018-03-19

Double Flexible Tip Wire Guides

Applicant Cook Incorporated

K-Number K171912

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HRS 2018-03-19

Anchorage Bone Plating System

Applicant Stryker GmbH

K-Number K172148

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NRY 2018-03-18

AXS Catalyst Distal Access Catheter 058 x 115cm; AXS Catalyst Distal Access Catheter 058 x 132cm; AXS Catalyst Distal Access Catheter 060 x 132cm

Applicant Stryker

K-Number K173841

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KGN 2018-03-16

XCelliStem Wound Powder

Applicant Stemsys

K-Number K172593

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KRH 2018-03-16

MEMO 4D

Applicant Sorin Group Italia S.R.L.

K-Number K180411

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NHA 2018-03-16

MIS CONNECT Conical Connection Abutment

Applicant Mis Implants Technologies , Ltd.

K-Number K173326

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HIF 2018-03-16

SurgiQuest AIRSEAL iFS System

Applicant Conmed Corporation

K-Number K172516

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DXN 2018-03-16

Microlife Upper Arm Automatic Digital Blood Pressure Monitor

Applicant Microlife Intellectual Property GmbH

K-Number K171937

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