MAUDE Adverse Event Report: ARTHREX, INC. BONE CUTR,HL 4.2MMX 19CM; BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

Model Number	BONE CUTR,HL 4.2MMX 19CM
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/16/2021
Type of Reportable Event	Malfunction
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.If the device becomes available for evaluation, a follow-up report will be submitted.
Event or Problem Description
It was reported during a hip arthroscopy as the surgeon was using the ar-6420bc for routine burring of a cam and pincer lesion, the blade snapped.Another blade was brought in to complete the procedure.

• Brand Name: BONE CUTR,HL 4.2MMX 19CM
• Common Device Name: BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• MDR Report Key: 11761178
• Report Number: 1220246-2021-02987
• Device Sequence Number: 11051256
• Product Code: GFA
• UDI-Device Identifier: 00888867039162
• UDI-Public: 00888867039162
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial
• Report Date (Section B): 05/03/2021

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 Number: BONE CUTR,HL 4.2MMX 19CM
• Device Catalogue Number: AR-6420BC
• Device Lot Number: 10145176
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/16/2021
• Initial Report FDA Received Date: 05/03/2021
• Patient Sequence Number: 1