MAUDE Adverse Event Report: ORTHOPEDIATRICS 5.5/6.0 UNIAXIAL PEDICLE SCREWS - Ø6.5MM, 40MM LENGTH

Model Number	00-1300-6640
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	03/09/2026
Type of Reportable Event	Malfunction
Event or Problem Description
1 year post op follow up patient showed with broken screw at liv.

• Brand Name: 5.5/6.0 UNIAXIAL PEDICLE SCREWS - Ø6.5MM, 40MM LENGTH
• Common Device Name: 5.5/6.0 UNIAXIAL PEDICLE SCREWS - Ø6.5MM, 40MM LENGTH
• Manufacturer (Section D): ORTHOPEDIATRICS; 2850 frontier drive; warsaw IN 46582
• Manufacturer (Section G): ORTHOPEDIATRICS, CORP; 2850 frontier drive; warsaw IN
• Manufacturer Contact: james gunnels ; 2850 frontier drive; warsaw, IN
• MDR Report Key: 24815667
• Report Number: 3006460162-2026-00016
• Device Sequence Number: 5952234
• Product Code: NKB
• UDI-Device Identifier: 00841132130674
• UDI-Public: 00841132130674
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K150600
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 04/08/2026

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
• Device Model Number: 00-1300-6640
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/11/2026
• Initial Report FDA Received Date: 04/08/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Male