DePuy
DePuy 1341-18 Kuntscher Nail Intramedullary Rod Curved 15mm x 46cm
DePuy 1341-18 Kuntscher Nail Intramedullary Rod Curved 15mm x 46cm
• Model: 1341-18
• Diameter: 15 mm
• Length: 46 cm (460 mm)
• Design: Curved
• Material: Stainless Steel
• Fixation Style: Classic non‑locking
The DePuy 1341-18 Küntscher Nail Intramedullary Rod 15 mm × 46 cm is a precision-engineered orthopedic implant designed to deliver dependable internal stabilization for adult long bone fractures, especially femoral diaphyseal breaks. Part of DePuy’s trusted orthopedic legacy, this curved intramedullary nail features a 15 mm diameter and 46 cm length tailored for substantial load sharing and alignment within the femoral medullary canal. Its anatomically contoured profile helps surgeons maintain natural bone geometry while providing structural integrity throughout the healing process — a critical advantage in long bone trauma care.
Built in the classic Küntscher nail style, this intramedullary rod promotes internal support without the need for external hardware, reducing soft tissue disruption compared to extramedullary fixation methods. The non-locking, solid design relies on snug press-fit engagement within the medullary canal to deliver reliable stabilization, making it especially effective in simple diaphyseal fracture patterns where rotational control can be managed clinically. This foundational fixation approach has stood the test of time in orthopedic trauma surgery.
Manufactured to meet rigorous surgical standards from high-strength, biocompatible materials, the DePuy 1341-18 Küntscher Nail integrates seamlessly into established operative workflows. Its durable construction and trusted intramedullary design offer surgeons and surgical teams confidence in achieving stable fracture fixation with predictable outcomes. Whether in acute trauma settings or complex reconstructive cases, this intramedullary rod remains a cornerstone solution for long bone fracture stabilization and effective patient rehabilitation
This medical supply or implant item's original equipment manufacturer (OEM) packaging has been compromised or opened. While it remains unused, it is listed as non-sterile and sterilization will be required prior to use.