Stryker Receives FDA Clearance for Q Guidance System for Spine Applications
Stryker Corporation (SYK)
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Source: Business Wire
Innovative planning and intraoperative platform designed to be a procedural ecosystem for surgeons and their patients during image-guided surgery KALAMAZOO, Mich.--(BUSINESS WIRE)--Stryker (NYSE:SYK) today announced that its Q Guidance System received 510(k) clearance from the U.S. Food and Drug Administration. The System, when used with the Spine Guidance Software, is an advanced planning and intraoperative guidance system designed to enable open or percutaneous computer-assisted surgery. The Spine Guidance Software is the first spine navigation software to receive clearance from the FDA for use with pediatric patients aged 13 and older.Stryker’s Q Guidance System aims to deliver surgical spine planning and navigation capability through multiple tracking options, sophisticated software algorithms and smart instrumentation. It features a high-performance navigation camera built on the company’s 20 years of experience developing guidance technologies. Q Guidance features completely
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Earnings
- 1/30/24 - Beat
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Sec Filings
- 3/26/24 - Form DEFA14A
- 3/26/24 - Form DEF
- 3/25/24 - Form 4
- SYK's page on the SEC website