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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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204 records meeting your search criteria returned- Product Code: MJO Patient Problem: Insufficient Information Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
LDR MÉDICAL MOBI-C IMPLANT M"STANDARD", UNKNOWN SIZE 11/01/2022
LDR MÉDICAL MOBI-C IMPLANT M"STANDARD", UNKNOWN SIZE 11/01/2022
LDR MÉDICAL MOBI-C IMPLANT M"STANDARD", UNKNOWN SIZE 10/07/2022
CENTINEL SPINE PRODISC C US IMPLANT 09/15/2022
SPINAL KINETICS LLC M6-C 09/14/2022
SPINAL KINETICS LLC M6-C 09/14/2022
SPINAL KINETICS LLC M6-C 09/14/2022
CENTINEL SPINE PRODISC L IMPLANT POLY INLAY 08/30/2022
CENTINEL SPINE PRODISC L IMPLANT INFERIOR PLATE 08/30/2022
CENTINEL SPINE PRODISC L IMPLANT SUPERIOR PLATE 08/30/2022
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