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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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43 records meeting your search criteria returned- Product Code: FQH Product Problem: Noise, Audible Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW MEDICAL LTD. VERSAJET II CONSOLE 11/06/2020
SMITH & NEPHEW MEDICAL LTD. VERSAJET II CONSOLE 10/30/2020
SMITH & NEPHEW MEDICAL LTD. VERSAJET II CONSOLE 10/28/2020
SMITH & NEPHEW MEDICAL LTD. VERSAJET II CONSOLE 06/17/2020
SMITH & NEPHEW MEDICAL LTD. VERSAJET II CONSOLE 05/22/2020
SMITH & NEPHEW MEDICAL LTD. VERSAJET II CONSOLE 05/22/2020
SMITH & NEPHEW MEDICAL LTD. VERSAJET II CONSOLE 12/13/2019
ZIMMER SURGICAL, INC. HIP KIT 01/24/2018
ZIMMER SURGICAL, INC. HIP KIT 12/05/2017
SMITH & NEPHEW MEDICAL LTD. VERSAJET II CONSOLE 09/04/2017
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