DePuy 1340-59 Kuntscher Nail Intramedullary Rod Curved 12mm x 32cm

DePuy 1340-59 Kuntscher Nail Intramedullary Rod Curved 12mm x 32cm

• Model: 1340-59
• Diameter: 12 mm
• Length: 32 cm (320 mm)
• Design: Curved
• Material: Stainless Steel
• Fixation Style: Classic non‑locking

The DePuy 1340‑59 Kuntscher Nail Intramedullary Rod Curved (12 mm × 32 cm) is a premium orthopedic implant engineered for dependable long bone fracture stabilization in trauma and reconstructive surgical procedures. Designed with a purposeful curvature, this intramedullary rod is optimized to follow the natural anatomical contour of long bones such as the femur and tibia, promoting smoother canal insertion and enhanced anatomical fit. Its robust 12 mm diameter and 32 cm length make it an excellent choice for adult patients requiring strong internal fixation where reliable alignment and support are paramount.

Manufactured to stringent quality standards from biocompatible materials, the DePuy 1340‑59 curved Kuntscher nail embodies the trusted engineering that orthopedic surgeons depend on for effective fracture management. The curved design helps distribute mechanical loads more evenly through the medullary canal, which can support physiological load sharing during healing and reduce the stress concentration that might occur with straight implants. As part of the classic Küntscher nailing approach, this rod supports internal alignment while minimizing surgical trauma compared with traditional external fixation methods.

Backed by DePuy Synthes’ longstanding reputation in orthopedic innovation, the DePuy 1340‑59 provides clinicians with a reliable solution tailored for challenging trauma scenarios. Whether used in closed reduction techniques or as part of comprehensive limb reconstruction strategies, this curved intramedullary rod combines proven design principles with dependable mechanical integrity — making it a robust choice for surgical teams focused on optimized long bone stabilization and improved patient outcomes.

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.