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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDTRONIC SOFAMOR DANEK USA, INC. Metrx; ARTHROSCOPE

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MEDTRONIC SOFAMOR DANEK USA, INC. Metrx; ARTHROSCOPE Back to Search Results
Model Number 9560100
Medical Device Problem Code Optical Problem (3001)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 07/15/2026
Type of Reportable Event Malfunction
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Brand Name
Metrx
Common Device Name
ARTHROSCOPE
Manufacturer (Section D)
MEDTRONIC SOFAMOR DANEK USA, INC.
4340 swinea rd
memphis TN 38118
Manufacturer (Section G)
MEDTRONIC SOFAMOR DANEK USA, INC.
4340 swinea rd
memphis TN 38118
Manufacturer Contact
justin ellis
1800 pyramid place
memphis, TN 38132
+1(763)526-5677
MDR Report Key50140615
Report Number3003120897-2026-01351
Device Sequence Number21513298
Product Code HRX
UDI-Device Identifier00885074210353
UDI-Public(01)00885074210353(11)201026(10)1560582
Combination Product (Y/N)N
Initial Reporter CountryJA
PMA/510(K) Number
K002931
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,User Facility
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 08/05/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model Number9560100
Device Catalogue Number9560100
Device Lot Number1560582
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer07/22/2026
Is the Reporter a Health Professional? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 07/22/2026
Initial Report FDA Received Date08/05/2026
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured10/26/2020
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Reuse
Patient Sequence Number1
Patient SexUnknown
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