drea MIS and open procedures - Carevature Medical · 2020. 5. 24. · drea MIS and open procedures...

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The only decompression system for the cervical spine MIS and open procedures drea Model: 2L75FU Osteophyte and ligament removal in ACDF Osteophyte removal following corpectomy Models: 3S45FUS | 3S45FU Uncusectomy and Foraminotomy in ACDF Model: 3L10DS The Dreal™ is intended to cut bone in neurosurgical and spinal applications. Prior to use, the surgeon should refer to the product Instructions for Use (IFU) for complete indications, warnings, precautions and contraindications.

Transcript of drea MIS and open procedures - Carevature Medical · 2020. 5. 24. · drea MIS and open procedures...

Page 1: drea MIS and open procedures - Carevature Medical · 2020. 5. 24. · drea MIS and open procedures ™ Model: 2L75FU Osteophyte and ligament removal in ACDF Osteophyte removal following

The only decompression system for the cervical spine MIS and open proceduresdrea ™

Model: 2L75FU

Osteophyte and ligament removal in ACDF

Osteophyte removal following corpectomy

Models: 3S45FUS | 3S45FU

Uncusectomy and Foraminotomy in ACDF

Model: 3L10DS

The Dreal™ is intended to cut bone in neurosurgical and spinal applications. Prior to use, the surgeon should refer to the productInstructions for Use (IFU) for complete indications, warnings, precautions and contraindications.

Page 2: drea MIS and open procedures - Carevature Medical · 2020. 5. 24. · drea MIS and open procedures ™ Model: 2L75FU Osteophyte and ligament removal in ACDF Osteophyte removal following

The Dreal™ device was used to remove the cartilage from the endplate in preparation for interbody or arthroplas-ty implant. The Dreal™ was useful in removing posterior osteophytes.All patients showed signi�cant improvement in Visual Analog Scale and Neck Disability Index from baseline to 1 day post-surgery. Complete bony resection was con�rmed in all patients using magnetic resonance imaging (MRI). No adverse events related to use of the Dreal™ device were reported.

A case series of 10 patients with cervical stenosis, who underwent anterior cervical discectomy and fusion (ACDF)or cervical disc arthroplasty, were evaluated. The Dreal™ was used to thin the uncus, allowing the remaining uncus to be removed with a Kerrison Rongeur. This in turn allowed for unobstructed access to the foramen for decompression.

Clinical Outcome Measures Before and After ACDFor Cervical Disc Arthroplasty Using the Dreal™Decompression System

NDI, Neck Disability Index; VAS, Visual Analog Scale

Safer access. Preserved bone. Better results.

*Pierre Bernard, M.D.(1), Michal Tepper, Ph.D.(2), Ely Ashkenazi, M.D.(3) [White Paper], Centre Aquitain du Dos, Hôpital Privé Saint Martin, France; Carevature Medical Ltd., Israel; The Israeli Spine Center, Assuta Medicle Center, Tel Aviv, Israel

Clinical experience*

100

80

60

40

20

0

-20VAS neck VAS arm NDI

53.0

18.4

PRE OPPOST OP

59.5

13.123.08

6.79

3S45FU 3S45FUSAdjacent Level Decompression following Corpectomy

2L75FU

ACDF osteophyte removalUncusectomy and Foraminotomy in ACDF

3L10DS

Uncusectomy and Foraminotomy in ACDFPosterior Cervical foraminotomy and laminectomy

MKT

029

01

Carevature® and Dreal™ are Registered Trademarks of Carevature Medical Ltd.

Carevature Medical, Inc. | 190 Industrial Road, Suite 2, Wrentham, MA 02093 U.S.www.carevature.com | Customer Services: 1-855-201-5770 | [email protected]