JACKSONVILLE, Fla., March 2 (HSMN NewsFeed) — OrthoDynamix announced today that it has received FDA clearance for its new device, ArthroSteer THREE.5mm Ablator, a mono polar electrosurgical device, for general surgical use, including the orthopedic and arth…
Devices, Orthopaedic, Surgery, FDA
OrthoDynamix, ArthroSteer
Posts on ‘March 2nd, 2010’
OrthoDynamix LLC Receives FDA 510(k) Clearance for ArthroSteer(R) 3.5mm Ablator
FDA Classifies Baxter’s January HomeChoice Peritoneal Dialysis Cycler Field Corrective Action as a Class I Recall
Baxter is Deploying Revised Labeling, Training and Upcoming Software Revisions to Further Assist Clinicians and Patients DEERFIELD, Ill.–(HSMN NewsFeed)–Baxter Healthcare Corporation announced today that the U.S. Food and Drug Administration (FDA) has…
Devices, Product Recall, FDA
Baxter, HomeChoice, peritoneal dialysis, home dialysis, dialysis

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