MAUDE Adverse Event Report: I.T.S. GMBH SPIRAL DRILL, PRS PHOENIX, D=2.7MM, L=305MM, AO CONNECTOR

Model Number	61273-305
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/15/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
We have inspected the dhf of the lot and the material certificate and the batch was processed through the normal manufacturing and inspection operations with no non-conformances or rework noted.The article met all dimensional and visual criteria at the time of release with no issues documented during the manufacture that would contribute to this complaint condition.Based on the information available, no final conclusion could be drawn and it has been determined that no corrective and preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If information is obtained that was not available for the initial medwatch, a follow up medwatch will be filed as appropriate.This report does not reflect a conclusion by fda, i.T.S.Gmbh or its employees that the report constitutes an admission that the device caused or contributed to the potential event described in this report.
Event or Problem Description
It was reported that multiple drills broke during surgery.This is report 4/4.

• Brand Name: SPIRAL DRILL, PRS PHOENIX, D=2.7MM, L=305MM, AO CONNECTOR
• Common Device Name: SPIRAL DRILL, PRS PHOENIX, D=2.7MM, L=305MM, AO CONNECTOR
• Manufacturer (Section D): I.T.S. GMBH; autal 28; lassnitzhoehe, styria 8301 ; AU 8301
• Manufacturer (Section G): I.T.S. GMBH; autal 28; lassnitzhoehe, styria 8301 ; AU 8301
• Manufacturer Contact: florian grill ; autal 28; lassnitzhoehe, styria 8301 ; AU 8301
• MDR Report Key: 18763826
• Report Number: 3004369035-2024-00104
• Device Sequence Number: 17258660
• Product Code: HTW
• UDI-Device Identifier: 09120069818109
• UDI-Public: 09120069818109
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K210935
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 02/22/2024

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: 61273-305
• Device Catalogue Number: 61273-305
• Device Lot Number: 23/223405
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 01/23/2024
• Initial Report FDA Received Date: 02/22/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 60 YR
• Patient Sex: Unknown
• Patient Weight: 86 KG