SBIR-STTR Award

Instruments for Endoscopic Intracranial Microsurgery
Award last edited on: 6/2/09

Sponsored Program
SBIR
Awarding Agency
NIH : NINDS
Total Award Amount
$502,723
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Miles Finn

Company Information

Clarus Medical LLC (AKA: Clarus Medical Systems~Medilase Inc)

1000 Boone Avenue North Suite 100
Minneapolis, MN 55427
   (763) 525-8400
   admin@clarus-medical.com
   www.clarus-medical.com
Location: Single
Congr. District: 05
County: Hennepin

Phase I

Contract Number: 1R43NS032611-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1994
Phase I Amount
$56,585
Awardee's statement of the potential commercial applications of the research:Novel endoscopic microsurgical instruments will be produced for the neurosurgery market. This project could lead to development of an instrument set that would be used by three-quarters of the nation's neurosurgeons.National Institute of Neurological Disorders and Stroke (NINDS)

Phase II

Contract Number: 2R44NS032611-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
1996
(last award dollars: 1997)
Phase II Amount
$446,138

The goal of this project is to develop a set of endoscopic surgical tools, designed specifically for neurosurgery. The instruments will include both curved and malleable versions, allowing them to be placed in "blind spots", where - without excessive retraction, neurosurgeons cannot normally see. Visualization will be provided by a removable endoscope. These instruments will allow application of "minimally-invasive surgical" techniques to neurosurgery. For example, they may help reduce morbidity in 45,000 spinal surgery procedures annually in the USA alone. A key goal is to develop reusable endoscopes to be used with the surgical instruments. The availability of reusable endoscopes, as compared to single-use models, will keep the cost of the equipment low, and will also reduce medical waste. The study methodology will include a clinical trial. Extensive testing, using industry-standard techniques, will be used to assure that an adequate sterilization assurance level is reached. The project will generate data concerning the proposed devices' safety and effectiveness, and these data will be used in a product clearance submission to the Food and Drug Administration following FDA clearance, Clarus will be prepared to commercialize these devices. PROPOSED COMMERCIAL APPLICATION: Suitable for 15% of lumbar spine discectomies--i.e. 45,000 procedures annually; many intracranial tumors (e.g. craniopharyngioma).