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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ARTHREX, INC. CLAV FRAC PLT,CENTRAL THIRD,LFT,SS; PLATE, FIXATION, BONE
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ARTHREX, INC. CLAV FRAC PLT,CENTRAL THIRD,LFT,SS; PLATE, FIXATION, BONE Back to Search Results
Model Number CLAV FRAC PLT,CENTRAL THIRD,LFT,SS
Health Effect - Clinical Code Failure of Implant (1924)
Date of Event 01/12/2021
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
The contribution of the device to the reported event could not be determined as the device was not returned for evaluation.The root cause of the event could not be determined from the information available and without device evaluation.
 
Event or Problem Description
It was reported through the fda's medwatch program that an ar-2652cl clavicle plate failed post-operatively.The patient felt a pop while driving and lifting his arm and his surgeon confirmed that the plate fractured at the previous fracture site.No facility or contact information was provided.
 
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Brand Name
CLAV FRAC PLT,CENTRAL THIRD,LFT,SS
Common Device Name
PLATE, FIXATION, BONE
Manufacturer (Section D)
ARTHREX, INC.
1370 creekside boulevard
naples FL 34108 1945
MDR Report Key11435696
Report Number1220246-2021-02669
Device Sequence Number16923474
Product Code HRS
UDI-Device Identifier00888867027428
UDI-Public00888867027428
Combination Product (Y/N)N
Initial Reporter StateFL
Initial Reporter CountryUS
PMA/510(K) Number
K143139
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2020
Reporter Type Manufacturer
Report Source user facility
Initial Reporter Occupation Administrator/Supervisor
Type of Report Initial
Report Date (Section B) 03/08/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device Health Professional
Device Model NumberCLAV FRAC PLT,CENTRAL THIRD,LFT,SS
Device Catalogue NumberAR-2652CL
Device Lot Number381610
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 02/15/2021
Initial Report FDA Received Date03/08/2021
Patient Sequence Number1
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