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510(k) Data Aggregation
(106 days)
The Subcutaneous Urinary Diversion Stent Set and Exchange Set is used to create a new tunnel leading from the renal pelvis to the urinary bladder for the purpose of providing decompression of the renal system.
The Subcutaneous Urinary Diversion Stent Set and Exchange Set is used to create a new tunnel leading from the renal pelvis to the urinary bladder for the purpose of providing decompression of the renal system. The set contains a stent, dilators, sheaths, wire guides, needle syringe and the exchange set contains a dilator, sheath, positioner, release sleeve and wire guide. This device is intended for one-time use.
The provided text is a 510(k) summary for a medical device (Subcutaneous Urinary Diversion Stent Set) submitted in 1996. This type of document, particularly from this era, does not contain the kind of detailed information about acceptance criteria, study design, and performance metrics that you are requesting.
510(k) submissions, especially those from the 1990s, focused primarily on demonstrating "substantial equivalence" to a predicate device. This typically involved comparing indications for use, technological characteristics (materials, design), and sometimes basic performance data. They were not clinical studies in the modern sense with specific acceptance criteria, ground truth establishment, or statistical power calculations for AI performance.
Therefore, I cannot provide the information requested from the input text because it is not present. The document focuses on demonstrating equivalence to predicate devices, not on a study proving the device meets specific performance acceptance criteria.
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