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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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66 records meeting your search criteria returned- Product Code: KWA Patient Problem: Damage to Ligament(s) Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BIOMET ORTHOPEDICS M2A-MAGNUM PF CUP 50ODX44ID 07/08/2014
BIOMET ORTHOPEDICS M2A-TAPER LINER SZ 41/28 06/30/2014
BIOMET ORTHOPEDICS M2A-MAGNUM PF CUP 52ODX46ID 06/19/2014
BIOMET ORTHOPEDICS M2A 38MM MOD HD +12MM NK SKRT 06/13/2014
BIOMET ORTHOPEDICS RECAP CEMENT FMRL HD RESUR 50M 06/05/2014
BIOMET ORTHOPEDICS M2A 38MM MOD HEAD -6MM NK 06/04/2014
BIOMET ORTHOPEDICS M2A-MAGNUM PF CUP 50ODX44ID 06/03/2014
BIOMET ORTHOPEDICS M2A-MAGNUM PF CUP 48ODX42ID 05/30/2014
BIOMET ORTHOPEDICS M2A-MAGNUM PF CUP 60ODX54ID 05/30/2014
BIOMET ORTHOPEDICS SELEX/MAGNUM MOD HD 40MM -6 05/28/2014
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