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To embed, copy and paste the code into your website or blog: The New Jersey Appellate Division has released a ruling categorically allowing evidence on FDA 510(k) clearance in medical device cases, reversing for new trials in two cases where that evidence was excluded. The court held that “evidence of such authorization does have probative value in evaluating the company s design and sale of the devices.” “Although several courts in other jurisdictions have chosen in their discretion to exclude such 510(k) evidence from jury trials involving the design and safety of mesh devices, we adopt the approach of other courts that have deemed such proof admissible with appropriate limiting instructions,” the decision states. “We are persuaded there is sufficient probative value of such evidence under N.J.R.E. 401 to justify informing the jurors, without extensive elaboration, that the products were reviewed by the FDA under the 510(k) clearance process before defendants sales in

Phil goldbergKatie mastrucciDan rogersNational association of manufacturersTechnology associationUs chamberJersey appellate divisionNew jersey appellate divisionPartner dan rogersAdvanced medical technology associationNational associationPartners phil goldbergபில் கோல்ட்பர்க்டான் ரோஜர்ஸ்தேசிய சங்கம் ஆஃப் உற்பத்தியாளர்கள்தொழில்நுட்பம் சங்கம்