VERTEX RECONSTRUCTION SYSTEM
Report
- Report Number
- 1030489-2015-01503
- 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
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).
IT WAS REPORTED BY (B)(6) 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 |
|---|---|---|---|---|---|---|---|
| 465837 | VERTEX RECONSTRUCTION SYSTEM | APPLIANCE, FIXATION, SPINAL INTERLAMINAL | KWP | MEDTRONIC SOFAMOR DANEK USA, INC | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |