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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS, INC. 1818910 ATTUNE DISTAL FEMORAL JIG 11/07/2017
MICROPORT ORTHOPEDICS INC. ACETABULAR CUP 11/06/2017
ZIMMER BIOMET, INC. ZIMMER UNICOMPARTMENTAL KNEE SYSTEM ARTI 11/05/2017
DEPUY ORTHOPAEDICS, INC. 1818910 SP*2 STD TB PUNCH GDE SZ 1.5-4 11/03/2017
ZIMMER BIOMET, INC. ZIMMER UNI ARTICULAR SURFACE PROVISIONAL 11/01/2017
DEPUY ORTHOPAEDICS, INC. 1818910 ATTUNE SHIM SZ7 5MM 11/01/2017
DEPUY ORTHOPAEDICS, INC. 1818910 ATTUNE SPACER BLOCK 10/31/2017
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL 10/31/2017
ASCENSION ORTHOPEDICS HUMERAL STEM TRIAL, 14MM 10/27/2017
ASCENSION ORTHOPEDICS STEM TRIAL HANDLE 10/27/2017
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