← Product Code [HWC](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HWC) · K093676 # OMNITECH LARGE, TRIMED COMPRESSION SCREW (K093676) _TriMed, Inc. · HWC · Mar 17, 2010 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HWC/K093676 ## Device Facts - **Applicant:** TriMed, Inc. - **Product Code:** [HWC](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HWC.md) - **Decision Date:** Mar 17, 2010 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3040 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use The TriMed Omnitech Large System is indicated for fracture fixation of large bone and large bone fragments, as well as fractures of the calcaneus, talus, and pelvis. ## Device Story TriMed Omnitech Large System consists of cannulated compression screws (4.5 mm and 7.3 mm diameters) used for bone fracture fixation. Screws feature dual thread pitches to draw distal bone fragments toward proximal fragments during insertion. Conical head design increases cortical bone contact area to prevent piercing and maintain compression. Used by surgeons in clinical/OR settings for orthopedic procedures. Device provides mechanical stabilization of bone fragments to facilitate healing. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Cannulated compression screws; diameters 4.5 mm and 7.3 mm; material: TA6V ELI titanium alloy (future option: stainless steel per ASTM F138); dual thread pitch; conical head design. ## Regulatory Identification A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system. ## Predicate Devices - Smith & Nephew Bone Plate System ([K993106](/device/K993106.md)/[K060736](/device/K060736.md)) - Synthes 7.0/7.3 mm Cannulated Screws ([K962011](/device/K962011.md)) - Synthes 4.5 mm Cannulated Screw ([K963172](/device/K963172.md)) ## 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}------------------------------------------------ K053676 ## MAR ] 7 2010 ### 510(K) Summary of Safety and Effectiveness TRIMED OMNITECH LARGE SYSTEM | Submitted By: | TriMed, Inc. | |-----------------------------|--------------------------------------| | | 25864 Tournament Road, Ste. A | | | Valencia, CA 91355 | | | (800)633-7221 | | Registration #: | 2031009 | | Manufactured By: | Biotech International | | | 305, allée de Craponne | | | 13300 Salon De Provence | | | France | | Registration#: | 3005270144 | | Prepared By/Contact Person: | Kelli Anderson | | | Phone: (661)312-7150 | | | Fax: (661)254-8485 | | Proprietary Name: | Omnitech Large or TriMed Compression | | | Screw | | Classification: | Class II: Bone, Fixation, Screws | | | HWC - Section 888.3040 | | | Class II: Pin, Fixation, Smooth | | | HTY - Section 888.3040 | | Summary Preparation Date: | March 10, 2010 | #### I. Indications for Use: . " ﺮ ﺍﻟﻤﺴﺎﺣﺔ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤ The TriMed Omnitech Large System is indicated for fracture fixation of large bone and large bone fragments, as well as fractures of the calcaneus, talus, and pelvis. {1}------------------------------------------------ #### Device Description: II. :"小 The Omnitech Large screws are cannulated titanium compression screws available in diameters of 4.5 mm and 7.3 mm. The screws utilize two different thread pitches allowing the distal fragment to be drawn towards the proximal fragment with each turn of the screw. The conical shaped head increases the surface contact area with the cortical bone avoiding piercing of the cortical bone and the subsequent loss of compression. Currently the screws are made of TA6V ELI titanium alloy. Surgical grade stainless steel screws complying with ASTM F138 may be made available in the future. #### III. Substantial Equivalence: K993106/K060736 - Smith & Nephew, Smith & Nephew Bone Plate System K962011- Synthes (USA), Synthes 7.0/7.3 mm Cannulated Screws K963172 - Synthes (USA), Synthes 4.5 mm Cannulated Screw {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized depiction of an eagle or bird with three wing-like strokes, positioned within a circle. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged around the circumference of the circle. Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002 TriMed. Inc. % Ms. Kelli Anderson Regulatory Affairs Consultant 25864 Tournament Road, Suite A Valencia, California 91355 MAR 1 7 2010 Re: K093676 Trade/Device Name: TriMed Omnitech Large System Regulation Number: 21 CFR 888.3040 Regulation Name: Smooth or threaded metallic bone fixation fastener Regulatory Class: II Product Code: HWC, HTY Dated: February 17, 2010 Received: February 22, 2010 Dear Ms. Anderson: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug. and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA), You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration. Ilsting of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set {3}------------------------------------------------ Page 2 - Ms. Kelli Anderson forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Sincerely vours. Qarban Buehno Mark N. Melkerson Director Division of Surgical, Orthopedic, and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ # Indications for Use 510(k) Number (if known):___K093676 Device Name:__________________________________________________________________________________________________________________________________________________________________ The TriMed Omnitech Large System is indicated for fracture fixation of large bone and large bone fragments, as well as fractures of the calcaneus, talus, and pelvis. Prescription Use (Part 21 CFR 801 Subpart D) . 、 AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Sarta for mxm (Division Sign-Off) (Division Sign-Off Division of Surgical. Orthopedic, and Restorative Devices 510(k) Number K093676 Page 1 of --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HWC/K093676](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HWC/K093676) **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