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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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29 records meeting your search criteria returned- Product Code: MBI Product Problem: Device Slipped Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. SELF BUNCHING KL 1.8 FIBERTAK, HIP 02/20/2023
ARTHREX, INC. SP FBRTAK RC TGRTPE WH/BLK & STTPE WH/BL 07/11/2022
ARTHREX, INC. FIBERTAK 07/05/2022
ARTHREX, INC. SP FIBERTAK RC, DBLOAD TAPE BL/W, BLK/W 06/20/2022
ARTHREX, INC. FIBERTAK 03/14/2022
ARTHREX, INC. H/W INTERNALBRACE LGMNT AUGMNT REPR KIT 01/18/2022
ARTHREX, INC. FIBERTAK 10/19/2021
ARTHREX, INC. H/W INTERNALBRACE LGMNT AUGMNT REPR KIT 10/12/2021
ARTHREX, INC. FIBERTAK 08/17/2021
ARTHREX, INC. IMPLANT SYSTEM, FIBERTAK BUTTON 06/28/2021
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