FDA Adverse Event Malfunction Summary report: N

MSP METATARSAL SHORTENING SYSTEM

MDR report key: 10313829 · Received July 23, 2020

Report

Report Number
3009540749-2020-00017
Event Type
Malfunction
Date Received
July 23, 2020
Date of Event
February 22, 2020
Report Date
July 23, 2020
Manufacturer
NEXTREMITY SOLUTIONS
Product Code
HRS
PMA / PMN Number
K140724
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 1

CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED BECAUSE IT REMAINS IMPLANTED. DEVICE HISTORY RECORDS RELATED TO THE EVENT WERE REVIEWED. THERE WERE NO NON-CONFORMANCES DETECTED THROUGH THE DEVICE HISTORY RECORD REVIEW. IF ADDITIONAL INFORMATION IS OBTAINED WHICH CHANGES THE OUTCOME OF THE INVESTIGATION, A FOLLOW-UP REPORT WILL BE FILED.

Description of Event or Problem · 1

IT WAS REPORTED A METATARSAL SHORTENING SYSTEM PROCEDURE WAS PERFORMED ON (B)(6) 2020. ON (B)(6) 2020 SURGEON REPORTED THE MSP PLATE CRACKED FROM THE SLIT PORTION TO THE DYNAMIC HOLE. THE PATIENT HAS NO PAIN AND THE PRODUCT REMAINS IMPLANTED. SURGEON IS MONITORING THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
779565 MSP METATARSAL SHORTENING SYSTEM PLATE HRS NEXTREMITY SOLUTIONS 168415217B

Patients

Seq Age Sex Outcome Treatment
1