FDA Adverse Event Injury Summary report: N

VERTEX RECONSTRUCTION SYSTEM

MDR report key: 4923347 · Received July 17, 2015

Report

Report Number
1030489-2015-01504
Event Type
Injury
Date Received
July 17, 2015
Date of Event
January 19, 2015
Report Date
June 19, 2015
Manufacturer
MEDTRONIC SOFAMOR DANEK USA, INC
Product Code
KWP
PMA / PMN Number
UNK
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

LITERATURE CITATION : NANCY E. EPSTEIN. "PRELIMINARY DOCUMENTATION OF THE COMPARABLE EFFICACY OF VITOSS VERSUS NANOSS BIOACTIVE AS BONE GRAFT EXPANDERS FOR POSTERIOR CERVICAL FUSION." (B)(6). (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED BY NANCY E. EPSTEIN IN A LITERATURE ARTICLE TITLED PRELIMINARY DOCUMENTATION OF THE COMPARABLE EFFICACY OF VITOSS VERSUS NANOSS BIOACTIVE AS BONE GRAFT EXPANDERS FOR POSTERIOR CERVICAL FUSION WAS REVIEWED FOR TWO SUCCESSIVE PROSPECTIVE COHORTS OF PATIENTS UNDERWENT 1-3 LEVEL LAMINECTOMIES WITH 5-9 LEVEL POSTERIOR CERVICAL FUSIONS TO ADDRESS CERVICAL SPONDYLOTIC MYELOPATHY (CSM) AND/OR OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT (OPLL). THE FIRST COHORT OF 72 PATIENTS RECEIVED VITOSS, WHILE THE SECOND COHORT OR 20 PATIENTS RECEIVED NANOSS. FUSIONS WERE PERFORMED UTILIZING THE ROD/EYELET SYSTEM WITH BRAIDED TITANIUM CABLES THROUGH THE BASE OF INTACT SPINOUS PROCESSES (NOT LATERAL MASS SCREWS) CEPHALAD AND CAUDAD TO LAMINECTOMY DEFECTS. THE AVERAGE AGES WERE, RESPECTIVELY, 63.3 (VITOSS) AND 62.5 (NANOSS). ONE TO THREE LEVEL LAMINECTOMIES (E.G. INCLUDING BILATERAL MEDIAL FACETECTOMY/FORAMINOTOMIES) WERE PERFORMED UNDER AN OPERATING MICROSCOPE UTILIZING DIAMOND DRILLS AND SMALL 1¿2 MM KERRISON RONGEURS TO REMOVE LATERAL BONE. THIS WAS FOLLOWED BY 5-9 LEVEL (E.G. TYPICAL C2-T2) ROD/EYELET FUSIONS PERFORMED UTILIZING BRADED TITANIUM CABLES (NO LATERAL MASS SCREWS) PASSED THROUGH THE BASE OF INTACT CEPHALAD/CAUDAD SPINOUS PROCESSES. THREE PATIENTS EXHIBITING DELAYED C5 ROOT PALSIES: IN TWO PATIENTS, C5 PALSIES WERE BILATERAL (BOTH ON DAY 2 IN ONE PATIENT, ON POSTOPERATIVE DAYS 2 AND 5, IN THE SECOND PATIENT); ONE WAS UNILATERAL OCCURRING ON POSTOPERATIVE DAY 3.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
464965 VERTEX RECONSTRUCTION SYSTEM APPLIANCE, FIXATION, SPINAL INTERLAMINAL KWP MEDTRONIC SOFAMOR DANEK USA, INC NA UNK

Patients

Seq Age Sex Outcome Treatment
1 Other