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The EVOS Cabling System is intended to be used in general orthopaedic repair procedures including patellar fractures, general cerclage, trochanteric reattachment, femoral and tibial fractures, prophylactic banding, olecranon fractures, ankle fractures, fixation of spiral fractures in conjunction with intramedullary nail and screw fixation techniques.

The EVOS Cabling System is used in orthopedic trauma and reconstructive surgeries to reduce and stabilize fractures and osteotomies. The EVOS Cabling System may be used for supplementary fracture fixation when used with bone plates or screws. The EVOS Cabling System includes a sterile, stainless-steel cable implant (ASTM F1314) packaged together with a stainless-steel crimp (ASTM F138). Non-sterile, reusable instruments are also provided to facilitate proper implantation of the cable-crimp implant.

This is a 510(k) summary for a medical device (EVOS Cabling System), not an AI/ML device. Therefore, the requested information regarding acceptance criteria, study details, ground truth, and sample sizes for AI/ML evaluation is not applicable and not present in the provided text.

The document discusses the substantial equivalence of the EVOS Cabling System to predicate devices based on non-clinical evidence. It outlines mechanical performance testing, MR safety evaluation, packaging and sterilization testing, biological safety evaluation, and pyrogenicity evaluation. However, these are standard device evaluation methods and not related to AI/ML performance.

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