MAUDE Adverse Event Report: I.T.S. GMBH STRAIGHT COMPRESSION PLATE, 10-HOLE

Model Number	21105-10
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Information (3190)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The device history record (dhr) of the straight compression plate (21105-10) was 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.Device was used for treatment, not diagnosis.
Event or Problem Description
It was reported that a straight compression plate, 10-hole was determined to be broken postoperatively.Original implant date unknown.A revision surgery was performed on an unknown date.

• Brand Name: STRAIGHT COMPRESSION PLATE, 10-HOLE
• Common Device Name: STRAIGHT COMPRESSION PLATE, 10-HOLE
• Manufacturer (Section D): I.T.S. GMBH; autal 28; lassnitzh?he, styria 8301 ; AU 8301
• MDR Report Key: 8572272
• Report Number: 3004369035-2017-00051
• Device Sequence Number: 16711401
• Product Code: HRS
• UDI-Device Identifier: 09120034309977
• UDI-Public: 09120034309977
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K060156
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 05/02/2019

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: 21105-10
• Device Catalogue Number: 21105-10
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 08/31/2017
• Initial Report FDA Received Date: 05/02/2019
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention