MAUDE Adverse Event Report: ARTHREX, INC. SUTR ANCH, BIO-COMP P-LCK, 2.4 X 11.3; SCREW, FIXATION, BONE

Model Number	SUTR ANCH, BIO-COMP P-LCK, 2.4 X 11.3
Health Effect - Clinical Code	Device Embedded In Tissue or Plaque (3165)
Date of Event	02/23/2021
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.
Event or Problem Description
It was reported that during a labral repair, six ar-2922bcs were used.One implanted fine, the other 5 broke during insertion.In all 5 attempts, the eyelet and an anchor fragment remains in the patient.Patient is 16 year old female.

• Brand Name: SUTR ANCH, BIO-COMP P-LCK, 2.4 X 11.3
• Common Device Name: SCREW, FIXATION, BONE
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• MDR Report Key: 11475192
• Report Number: 1220246-2021-02708
• Device Sequence Number: 2965742
• Product Code: HWC
• UDI-Device Identifier: 00888867197664
• UDI-Public: 00888867197664
• Combination Product (Y/N): N
• Initial Reporter State: OH
• Initial Reporter Country: US
• PMA/510(K) Number: K063479
• 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): 03/12/2021

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?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 10/31/2022
• Device Model Number: SUTR ANCH, BIO-COMP P-LCK, 2.4 X 11.3
• Device Catalogue Number: AR-2922BC
• Device Lot Number: 12208063
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/23/2021
• Initial Report FDA Received Date: 03/12/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1