← Product Code [HSB](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB) · K932330 # TI-6AL-7NB URTN (K932330) _Synthes (Usa) · HSB · Mar 8, 1996 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K932330 ## Device Facts - **Applicant:** Synthes (Usa) - **Product Code:** [HSB](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB.md) - **Decision Date:** Mar 8, 1996 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3020 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use Synthes Titanium-6Aluminum-7Niobium Unreamed Tibial Nail is intended for use in stabilizing fractures of the tibia. ## Device Story Titanium-6Aluminum-7Niobium alloy intramedullary nail; used for stabilization of tibial fractures. Device features proximal 9° sagittal angulation; allows interlocking with locking bolts. Diameters 8mm-9mm; lengths 255mm-420mm. Implanted by orthopedic surgeons in clinical/OR settings. Provides mechanical fixation to support bone healing. Modified from stainless steel predicate to improve anatomic fit and insertion characteristics. ## Clinical Evidence Bench testing only. Sterilization validated via AAMI Biological Indicator - Overkill Method for Low Bioburden Medical Devices, achieving sterility assurance level >10⁻⁶. ## Technological Characteristics Material: Titanium-6Aluminum-7Niobium alloy. Form factor: Intramedullary nail, 8-9mm diameter, 255-420mm length. Features: 9° proximal sagittal angulation, interlocking bolt capability. Sterilization: Gamma radiation (2.5-3.2 MegaRads) per AAMI guidelines. Packaging: Double-barrier PETG trays with Tyvek lids. ## Regulatory Identification An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures. ## Predicate Devices - Synthes Unreamed Tibial Nail ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0} SYNTHES KG32330 MAI: -8 Attachment VI: Summary of Safety and Effectiveness Information [510(k) Summary] Synthes (USA) (215) 647-9700 1690 Russell Road Contact: Diane Cochet-Wynant Paoli, PA 19301 May 12, 1993 Device: Synthes Titanium-6Aluminum-7Niobium Unreamed Tibial Nail, as compared to Synthes Unreamed Tibial Nail (stainless steel) Synthes Titanium-6Aluminum-7Niobium Unreamed Tibial Nail is intended for use in stabilizing fractures of the tibia. It is available in diameters of 8mm - 9mm, and lengths from 255mm to 420mm. The nail has a proximal angulation of 9° in the sagittal plane; it allows for interlocking with locking bolts. Synthes Unreamed Tibial Nail is also indicated for fractures of the tibia. To facilitate insertion and anatomic fit, the Unreamed Tibial Nail was modified (e.g., locking hole number/placement, material) to make the Titanium-6Aluminum-7Niobium Unreamed Tibial Nail. The method used to sterilize the Synthes Titanium-6Aluminum-7Niobium Unreamed Tibial Nail is gamma radiation, as recognized by the United States Pharmacopeia. The method used to validate the sterilization cycle was the Biological Indicator - Overkill Method for Low Bioburden Medical Devices per guidelines established by the Association for Advancement of Medical Instrumentation (AAMI). Synthes applied the guidelines appearing in "Process Control Guidelines for Gamma Radiation Sterilization of Medical Devices," AAMI, October 18, 1991. The AAMI Biological - Overkill Method dictates a sterility assurance level in excess of 10⁻⁶ which assures a 12 logarithmic reduction in a possible micro-organism population. The packaging system used to maintain device sterility consists of two sealed trays, one within the other, providing a double sterility barrier. The packaging trays and lids are manufactured from industry accepted components for EO and gamma radiation, namely, medical grade, blue tint, 6763 PETG plastic for the trays and Tyvek 1073 B for the lids. The sealed trays are placed in a paperboard shipping carton and shrink wrapped. The radiation dose used to insure sterility basis, is 2.5 - 3.2 MegaRads. The validation minimum dose range, per AAMI, is 1.8 - 2.6 MegaRads. --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K932330](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K932330) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com