MAUDE Adverse Event Report: I.T.S. GMBH CORTICAL SCREW, D=3.5MM, L=50MM

Model Number	32351-50
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	No Information (3190)
Date of Event	04/20/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device history record (dhr) of the affected lot of the 32351-50 screw were inspected and showed no deviations.The quality forms met all dimensional and visual criteria at the time of release with no issues documented during the manufacturing that would contribute to this complaint condition.A review of the raw material device history record revealed no deviation.The material was determined to be conforming and was used as is per product development approval.As a result of the above and the fact that no device was returned for evaluation, this complaint is deemed unconfirmed.This is report 2 of 2.
Event or Problem Description
It was reported that two non-locking cortical screws broke during an acetabular fixation.No medical intervention was needed and no delay of procedure.This is report 2 of 2.

• Brand Name: CORTICAL SCREW, D=3.5MM, L=50MM
• Common Device Name: CORTICAL SCREW, D=3.5MM, L=50MM
• Manufacturer (Section D): I.T.S. GMBH; autal 28; lassnitzh?he, styria 8301 ; AU 8301
• MDR Report Key: 10027913
• Report Number: 3004369035-2020-00052
• Device Sequence Number: 16335128
• Product Code: HWC
• UDI-Device Identifier: 09120047294260
• UDI-Public: 09120047294260
• Combination Product (Y/N): N
• PMA/510(K) Number: K063166
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 05/06/2020

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 Number: 32351-50
• Device Catalogue Number: 32351-50
• Device Lot Number: 18/192028
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/22/2020
• Initial Report FDA Received Date: 05/06/2020
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other