MAUDE Adverse Event Report: KARL LEIBINGER MEDIZINTECHNIK GMBH & CO. KG DISTRACTION

Model Number	51-361-30-09
Medical Device Problem Code	Mechanical Problem (1384)
Health Effect - Clinical Code	Impaired Healing (2378)
Date of Event	01/10/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Reference exemption number e2017029.
Event or Problem Description
It was reported that the distractor was sticking.The distractor was removed and replaced.
Additional Manufacturer Narrative
An investigation was performed using lab analysis which revealed only surface damage and bending.Device function was tested and there was no failure detected.The complaint percentage was not calculated and the device history records and risk files were not reviewed, as no product failure was found.The root cause cannot be determined due to no device failure being found.If further information is obtained that might add value to the contents of the investigation report, an additional follow-up report will be submitted.

• Brand Name: DISTRACTION
• Common Device Name: DISTRACTION
• Manufacturer (Section D): KARL LEIBINGER MEDIZINTECHNIK GMBH & CO. KG; kolbinger strasse 10; muehlheim/donau, 78570 ; GM 78570
• MDR Report Key: 8298198
• Report Number: 9610905-2019-00014
• Device Sequence Number: 1946804
• Product Code: MQN
• UDI-Device Identifier: 00888118080516
• UDI-Public: (01)00888118080516
• Combination Product (Y/N): N
• Initial Reporter State: KY
• Initial Reporter Country: US
• PMA/510(K) Number: K010139
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 01/10/2019
• Report Date (Section F): 01/10/2019

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: 51-361-30-09
• Device Lot Number: 33281468
• Was Device Available for Evaluation?: No
• Date Returned to Manufacturer: 01/23/2019
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 02/14/2019
• Event Location: Hospital
• Date Report to Manufacturer: 01/10/2019
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/10/2019
• Supplement Date Received by Manufacturer: 02/14/2019
• Initial Report FDA Received Date: 02/01/2019
• Supplement Report FDA Received Date: 02/25/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 17 YR