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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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42 records meeting your search criteria returned- Product Code: MBI Product Problem: Defective Device Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. KL 1.8 FIBERTAK, SHOULDER 03/29/2024
ARTHREX, INC. KL 1.8 FIBERTAK, SHOULDER 03/29/2024
ARTHREX, INC. IMPLANT SYSTEM, SUTURELOC 03/20/2024
ARTHREX, INC. FIBERTAG TIGHTROPE II WITH INTERNALBRACE 03/12/2024
ARTHREX, INC. SELF BUNCHING KL 1.8 FIBERTAK, HIP 02/28/2024
ARTHREX, INC. SP FBRTAK RC FBRTPE BLK/BLU & STTPE BLU 02/28/2024
ARTHREX, INC. KL FBTK RC, (WH/BLK)TT & (BLU)#2 MTS 02/23/2024
ARTHREX, INC. DX SWIVELOCK SL, 3.5X8.5MM W/FORK EYELET 01/29/2024
ARTHREX, INC. H/W INTERNALBRACE LGMNT AUGMNT REPR KIT 01/29/2024
ARTHREX, INC. SUTR ANCH,PEEK CRKSCRW FT,TRI-PLAY 01/23/2024
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