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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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13 records meeting your search criteria returned- Product Code: KWI Product Problem: Nonstandard Device Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ACUMED LLC ARH SLIDE-LOC¿ STANDARD STEM 10MM 03/19/2019
ACUMED LLC ARH SLIDE-LOC¿ NECK +1MM 03/19/2019
ACUMED LLC ARH SLIDE-LOC HEAD 22MM, LEFT 03/19/2019
ACUMED LLC ARH SOLUTIONS HEAD 12/14/2018
ACUMED LLC ARH SOLUTIONS STEM 12/14/2018
ACUMED LLC PROSTHESIS, ELBOW, HEMI-, RADIAL, STEM 12/14/2018
ACUMED LLC ARH SLIDE-LOC¿ NECK +1MM 07/18/2018
ACUMED LLC ARH SLIDE-LOC¿ STANDARD STEM 10MM 07/18/2018
ACUMED LLC ARH SLIDE-LOC HEAD 26MM, LEFT 07/18/2018
ACUMED LLC PROSTHESIS, ELBOW, HEMI-, RADIAL, HEAD 07/17/2018
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