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510(k) Data Aggregation
(69 days)
The SyndesMetrics Syndesmosis Repair System is intended for repair in the ankle including indications for:
Ankle syndesmosis fixation (syndesmosis disruptions), and as an adjunct in connection with trauma hardware for Weber B and C ankle fractures.
The SyndesMetrics Syndesmosis Repair System consists of a Fibular Anchor and a Tibial Anchor which are connected by a length of suture. The implant is marketed with previously cleared ultra-high molecular weight polyethylene (UHMWPE) 3.5mm OrthoTape® (K150438) which is provided sterile packaged from Teleflex, Inc.
The provided text describes a medical device, the SyndesMetrics Syndesmosis Repair System, and its 510(k) submission to the FDA. It does not contain information about acceptance criteria or a study proving the device meets acceptance criteria in the context of an AI/ML device.
The document is a 510(k) clearance letter for a physical medical device (SyndesMetrics Syndesmosis Repair System) that is intended for ankle syndesmosis fixation. The clearance is based on substantial equivalence to predicate devices, and the supporting data are non-clinical (mechanical testing).
Therefore, I cannot provide the requested information because the input text does not describe an AI/ML-based device or a study with acceptance criteria related to its performance. The "Nonclinical Testing" section explicitly states: "Clinical data were not needed to support the safety and effectiveness of the subject device."
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