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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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168 records meeting your search criteria returned- Product Code: HWT Patient Problem: No Patient Involvement Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. PROVISIONAL ARTICULAR SURFACE SIZE GREEN 01/22/2021
ZIMMER BIOMET, INC. ARTICULAR SURFACE PROVISIONAL SIZE E 14 12/17/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 3 8MM 11/20/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 2 8MM 11/20/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 4 8MM 11/19/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 2 8MM 11/16/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 2 10MM 11/16/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 3 9MM 11/16/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 5 8MM 11/11/2020
SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 6 8MM 11/11/2020
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