FDA Adverse Event Injury Summary report: N

SCREW, FIXATION, BONE

MDR report key: 5029038 · Received August 25, 2015

Report

Report Number
2520274-2015-15433
Event Type
Injury
Date Received
August 25, 2015
Report Date
August 18, 2015
Manufacturer
SYNTHES USA
Product Code
HWC
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. LI S.L., LU Y., WANG M.Y. (2015) IS CROSS-SCREW FIXATION SUPERIOR TO PLATE FOR RADIAL NECK FRACTURES? THE BONE AND JOINT JOURNAL;97-B:830-835. THIS REPORT IS FOR UNKNOWN HEADLESS CANNULATED SCREWS, UNKNOWN QUANTITY, UNKNOWN LOT. (B)(4). THE INVESTIGATION COULD NOT BE COMPLETED AND NO CONCLUSION COULD BE DRAWN, AS NO DEVICE WAS RETURNED AND NO LOT NUMBER OR PERT NUMBER WAS PROVIDED.

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING LITERATURE ARTICLE, LI S.L., LU Y., WANG M.Y.(2015). IS CROSS-SCREW FIXATION SUPERIOR TO PLATE FOR RADIAL NECK FRACTURES? BONE JOINT J 2015;97-B:830-5. THIS STUDY COMPARES THE OUTCOMES OF TWO METHODS OF FIXATION OF DISPLACED FRACTURES OF THE RADIAL NECK. THE 58 PATIENTS WITH A MEAN AGE OF 38.5 YEARS (18 TO 56), WERE TREATED IN A NONRANDOMISED STUDY WITH SCREWS (N = 29) OR A PLATE AND SCREWS (N = 29) ACCORDING TO THE SURGEON'S PREFERENCE. THE PATIENTS WERE REVIEWED AT ONE YEAR. RADIOGRAPHS AND FUNCTIONAL EVALUATIONS WERE CARRIED OUT UP TO ONE YEAR POST-OPERATIVELY, USING THE BROBERG AND MORREY FUNCTIONAL EVALUATION SCORE, RANGE OF MOVEMENT, AND ASSESSMENT OF COMPLICATIONS. RESULTS: ALL FRACTURES HEALED WITHIN FOUR MONTHS OF SURGERY. THERE WERE NO WOUND INFECTIONS, NERVE INJURIES, LOSS OF REDUCTION, OR FAILURES OF FIXATION IN ANY PATIENTS. FOUR PATIENTS DEVELOPED HETEROTOPIC OSSIFICATION AT THREE TO FOUR MONTHS POSTOPERATIVELY, OF WHICH ONE (3.4%) WAS IN THE SCREW GROUP AND THREE (10.3%) WERE IN THE PLATE GROUP (FISHER'S EXACT TEST, P = 0.61). THIS IS REPORT #1 OF 2 FOR (B)(4). THIS REPORT IS FOR UNKNOWN HEADLESS CANNULATED SCREWS AND REFERS TO THE HETEROTOPIC OSSIFICATION AT THREE TO FOUR MONTHS POSTOPERATIVELY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
561001 SCREW, FIXATION, BONE HWC SYNTHES USA

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention