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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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11 records meeting your search criteria returned- Product Code: NJL Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ATTUNE PS FB INSRT SZ 4 5MM 11/14/2022
DEPUY IRELAND - 9616671 ATTUNE PS FB INSRT SZ 6 7MM 09/14/2022
DEPUY IRELAND - 9616671 ATTUNE CRS FB INSRT SZ 3 10MM 08/30/2022
DEPUY IRELAND - 9616671 ATTUNE CR FB INSRT SZ 6 5MM 07/28/2022
DEPUY IRELAND - 9616671 ATTUNE PS FB INSRT SZ 8 8MM 07/25/2022
DEPUY IRELAND - 9616671 ATTUNE PS RP INSRT SZ 8 8MM 07/01/2021
DEPUY IRELAND - 9616671 ATTUNE PS RP INSRT SZ5 5MM 02/11/2021
DEPUY IRELAND - 9616671 ATTUNE PS RP INSRT SZ5 5MM 02/10/2020
DEPUY ORTHOPAEDICS INC US LCS COMPLETE M/B PAT POR LG+ 06/24/2019
DEPUY IRELAND - 9616671 ATTUNE PS RP INSRT SZ6 6MM 06/18/2019
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