MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 03,07 report with the FDA on 2014-02-26 for manufactured by Synthes Usa.

Event Text Entries

[4197470] Journal article received: early experience treating thoracic disc herniations using a modified transfacet pedicle-sparing decompression and fusion; richard bransford, fangyi zhang, carlo bellabarba, mark konodi, and jens r. Chapman; j neurosurg; department of orthopaedics and sports medicine, harborview medical center and department of neurosurgery, university of washington. : j neurosurg spine 12:221? 231, 2010; reported: the objective of this study was to assess outcomes and complications in a consecutive series of patients with thoracic disc herniations undergoing posterior transfacet decompression and discectomy with posterior instrumentation and fusion. Segmental fixation was performed with the universal spine system (synthes). Interbody arthrodesis was accomplished with machined freeze-dried allograft t-plif spacers (synthes). The average t-plif height was 9mm (range 7-15mm). Arthrodesis was carried out with a mixture of local bone graft derived from the neural element decompression, tricalcium phosphate pellets (chronos, synthes), demineralized bone matrix allograft (dbx, synthes), and autologous blood. Care was taken to ensure that approximately half of the graft material was composed of morcellized local bone graft. Results: eighteen consecutive patients with 29 symptomatic thoracic disc herniations were treated with a modified transfacetal, pedicle-sparing decompression and segmental reconstruction and fusion. The mean age of the patients was 50 years (range 27-71 years) and 11 of 18 were men. Three patients had postoperative infections. In all 3 cases, prolonged postoperative wound drainage required reoperation despite appropriate preoperative and postoperative intravenous antibiotic therapy. Each patient had positive bacterial cultures and responded successfully to operative irrigation and debridement and appropriate antibiotic therapy. An additional patient developed a large seroma that required percutaneous drainage under ct guidance. In another patient, postoperative imaging revealed an excessively long screw at t-6 in close proximity to the aorta. This patient also had a suboptimally placed allograft spacer within the t6-7 disc space and underwent an uneventful reoperation for repositioning of the left t-6 screw and the t6-7 allograft spacer on the second postoperative day; he was subsequently discharged 8 days after his original surgery. Two of the three patients who developed post-operative infections were at increased risk due to morbid obesity with body mass index greater than 35. Another patient was at increased risk due to poorly controlled diabetes. Conclusion: a modified transfacetal pedicle-sparing approach combined with short segmental fusion offers a safe means of achieving concurrent decompression and segmental stabilization and is an option for certain subtypes of thoracic disc herniation. Although 5 patients required additional surgery for postoperative complications, all patients experienced improvement relative to their preoperative status. This report is for an unknown rod. This report is 3 of 6 for (b)(4).
Patient Sequence No: 1, Text Type: D, B5


[11630730] Device is used for treatment, not diagnosis. Date of event: j neurosurg spine 12:221? 231, 2010. Device is an unknown rod, quantity 1. Investigation could not be completed, no conclusion could be drawn as no device was returned and no lot number was provided. Manufacturing records could not be reviewed without a lot number.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2520274-2014-00854
MDR Report Key3648469
Report Source03,07
Date Received2014-02-26
Date of Report2014-01-31
Date Mfgr Received2014-01-31
Date Added to Maude2014-02-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactLINDA PLEWS
Manufacturer Street1302 WRIGHTS LANE EAST
Manufacturer CityWEST CHESTER PA 19380
Manufacturer CountryUS
Manufacturer Postal19380
Manufacturer Phone8006207025
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Product CodeJDN
Date Received2014-02-26
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSYNTHES USA
Manufacturer AddressWEST CHESTER PA


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2014-02-26

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.