MAUDE Adverse Event Report: MEDOS INTERNATIONAL SÃ RL CH 5.5 EXP VERSE FEN SCR 7.0X40; BONE CEMENT, POSTERIOR SCREW AUGMENTATION

Model Number	199723740
Medical Device Problem Code	Device Slipped (1584)
Health Effect - Clinical Codes	Failure of Implant (1924); No Code Available (3191)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Additional device product code: mni.Complainant part is not expected to be returned for manufacturer review/investigation.(b)(4).Without a lot number, the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective, and/or preventative action is proposed.This complaint will be accounted for, and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
Device report from synthes reports an event in (b)(6) as follows: it was reported that the implants from a previous posterior lumbar interbody fusion (plif) surgery performed on (b)(6) 2020 were removed on (b)(6) 2020 due to subsidence of the cage and loosening of the screws.L4-plevis revision procedure was completed on on (b)(6) 2020.No further information provided.This report is for one (1) 5.5 exp verse fen scr 7.0x40.This is report 3 of 10 for complaint (b)(4).Additional devices are reported under related complaint (b)(4).

• Brand Name: 5.5 EXP VERSE FEN SCR 7.0X40
• Common Device Name: BONE CEMENT, POSTERIOR SCREW AUGMENTATION
• Manufacturer (Section D): MEDOS INTERNATIONAL SÃ RL CH; chemin-blanc 38; le locle 02400 ; SZ 02400
• MDR Report Key: 10805092
• Report Number: 1526439-2020-02118
• Device Sequence Number: 3204637
• Product Code: PML
• UDI-Device Identifier: 10705034402925
• UDI-Public: (01)10705034402925
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K160879
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 10/10/2020

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?: Yes
• Operator of Device: Health Professional
• Device Model Number: 199723740
• Device Catalogue Number: 199723740
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 10/10/2020
• Initial Report FDA Received Date: 11/06/2020
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention