FDA Adverse Event Injury Summary report: N

BONE PLATE

MDR report key: 5543637 · Received April 4, 2016

Report

Report Number
2520274-2016-11920
Event Type
Injury
Date Received
April 4, 2016
Date of Event
December 5, 2008
Report Date
March 7, 2016
Manufacturer
SYNTHES USA
Product Code
JEY
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THIS REPORT IS FOR AN UNKNOWN DISTRACTOR/UNKNOWN QUANTITY/UNKNOWN LOT. UDI IS UNAVAILABLE. THE INVESTIGATION COULD NOT BE COMPLETED AND NO CONCLUSION COULD BE DRAWN, AS NO DEVICE WAS RETURNED AND NO LOT NUMBER OR PART NUMBER WAS PROVIDEDIF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING LITERATURE ARTICLE WHITE IN 2008. POSTERIOR CALVARIAL VAULT EXPANSION USING DISTRACTION OSTEOGENESIS. CHILDS NERV SYST, 25:231-236. (B)(6). SIX PATIENTS UNDERWENT DISTRACTION OSTEOGENESIS OF THEIR POSTERIOR CALVARIAL DISTRACTION. DATA WAS PROSPECTIVELY COLLECTED FOR SIX PATIENTS, WHO UNDERWENT OSTEOGENESIS OF THEIR POSTERIOR CALVARIAL VAULT FOR RAISED INTRACRANIAL PRESSURE SECONDARY TO SYNDROMIC MULTISUTURE CRANIOSYNOSTOSIS BETWEEN OCTOBER 2006 AND JULY 2007. THE MEAN AGE AT TIME OF SURGERY WAS 1 YEAR 3 MONTHS. THE MEAN PERIOD OF DISTRACTION WAS 28 DAYS. DATA WAS COLLECTED FOR THE LENGTH OF THE DISTRACTION PERIOD, THE LENGTH OF THE CONSOLIDATION PERIOD AND THE DISTANCE OF THE ADVANCEMENT ACHIEVED. THREE INTERNAL 30 MM TITANIUM SINGLE VECTOR DISTRACTORS (SYNTHES,(B)(4)) WERE USED IN FOR EACH CASE. THERE WERE TWO LATERAL DISTRACTORS DISTRACTORS WERE POSITIONED IN EACH TEMPORAL REGION AND A SUPERIOR ONE PLACED OFF CENTER TO AVOID THE SAGITTAL SINUS. THIS REPORT IS FOR AN UNKNOWN DISTRACTOR AND REFERS TO THE FOLLOWING; CASE (B)(6) MALE EXPERIENCED LOOSENING OF A DISTRACTOR FOOTPLATE. THE DISTRACTORS WERE REMOVED. THIS IS REPORT 7 OF 7 FOR (B)(4). A COPY OF THIS LITERATURE ARTICLE IS BEING SUBMITTED WITH THIS MEDWATCH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
201470 BONE PLATE JEY SYNTHES USA

Patients

Seq Age Sex Outcome Treatment
1 9 MO Required Intervention