MAUDE Adverse Event Report: ARTHREX, INC. IMPL DELIVERY SYS,TRIM-IT SPIN PIN; PIN, FIXATION, SMOOTH

Model Number	IMPL DELIVERY SYS,TRIM-IT SPIN PIN
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/22/2022
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
On 6/23/2022, it was reported by a distributor via sems that an ar-4156ds trim-it spin pin metal portion, snapped off during insertion.All broken pieces were retrieved and case was completed without further issues.This was discovered during a toe realignment procedure on (b)(6) 2022.

• Brand Name: IMPL DELIVERY SYS,TRIM-IT SPIN PIN
• Common Device Name: PIN, FIXATION, SMOOTH
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• Manufacturer (Section G): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• Manufacturer Contact: vik bajnath ; 8009337001
• MDR Report Key: 14976761
• Report Number: 1220246-2022-05213
• Device Sequence Number: 5689864
• Product Code: HTY
• UDI-Device Identifier: 00888867032859
• UDI-Public: 00888867032859
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K050259
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Distributor
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial
• Report Date (Section B): 07/11/2022

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 Expiration Date: 03/31/2023
• Device Model Number: IMPL DELIVERY SYS,TRIM-IT SPIN PIN
• Device Catalogue Number: AR-4156DS
• Device Lot Number: 13116249
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/23/2022
• Initial Report FDA Received Date: 07/11/2022
• Date Device Manufactured: 04/14/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown