← Product Code [HRS](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS) · K070170 # DALL-MILES SYSTEM (K070170) _Stryker Orthopaedics · HRS · Mar 2, 2007 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K070170 ## Device Facts - **Applicant:** Stryker Orthopaedics - **Product Code:** [HRS](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS.md) - **Decision Date:** Mar 2, 2007 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3030 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use The subject devices are sterile, single use devices. They are intended for use during cemented or cementless primary or revision hip arthroplasty and trochanteric osteotomy. The Stainless Steel alloy Grip and Grip Plates are intended for use with 2.0mm Stainless Steel beaded and nonbeaded Cables only. Wrought CoCr alloy Grip and Grip Plates are intended for use with 2.0mm CoCr beaded and non-beaded Cables only. Optional Stainless Steel and Titanium screws are also available for use with the Stainless Steel and Wrought CoCr Grip Plates, respectively. ## Device Story Dall-Miles® System components, including Trochanteric Grips and Grip Plates, facilitate reattachment and fixation of the greater trochanter during hip arthroplasty or osteotomy. Devices are implanted by orthopedic surgeons in an operating room setting. The system utilizes metallic grips, plates, cables, and screws to provide mechanical stabilization of bone fragments. Stainless steel or CoCr alloy components are secured to the bone to maintain alignment during healing. The system is compatible with existing Dall-Miles® components, allowing surgeons to customize fixation based on patient anatomy and surgical requirements. Benefits include stable bone fixation, supporting recovery following hip procedures. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Metallic bone fixation system consisting of Trochanteric Grips and Grip Plates. Materials: Stainless Steel or Wrought CoCr alloy. Includes optional Stainless Steel or Titanium screws and 2.0mm beaded/non-beaded cables. Mechanical fixation principle. Sterile, single-use. No software or electronic components. ## Regulatory Identification Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system. ## Predicate Devices - Modified BMP™ Trochanteric Plates ([K993510](/device/K993510.md)) - Dall-Miles® Trochanter Cable Super Grip ([K962162](/device/K962162.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}------------------------------------------------ # MAR 0 2 2007 # 510(k) Summary of Safety and Effectiveness for the Dall-Miles® System | Proprietary Name: | Dall-Miles® System | |-----------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Common Name: | Bone Fixation Accessories | | Classification Name and Reference | Single/multiple component metallic bone fixation
appliances and accessories
Title 21 CFR §888.3030 | | | Bone fixation cerclage
Title 21 CFR § 888.3010 | | Regulatory Class: | Class II | | Device Product Code(s): | HRS - Plate, fixation, bone | | | LYT -- Fixation accessory | | | JDQ - Cerclage, fixation | | For Information Contact: | Patricia Setti-LaPerch
Regulatory Affairs Associate
Stryker Orthopaedics
325 Corporate Drive
Mahwah, New Jersey 07430
Phone: (201) 831-5938
Fax: (201) 831-4938
E-Mail: Patricia.LaPerch@stryker.com | | Date Summary Prepared: | January 16, 2007 | ### Device Description The Dall-Miles® product line will now be available with Trochanteric Grip Plates and Trochanteric Grips that facilitate reattachment and fixation of the Greater Trochanter. The Trochanteric Grips will be offered in small, medium, and large sizes. The Trochanteric Grip Plates will be offered in medium sizes ranging from 100-200mm and large sizes ranging from 110-210mm in length. Both the Trochanteric Grips and Grip Plates are compatible with the existing components of the Dall-Miles® System and will be available in Stainless Steel or CoCr alloy materials and packaging options with or without Cables. {1}------------------------------------------------ #### Intended Use: The subject devices are sterile, single use devices. They are intended for use during cemented or cementless primary or revision hip arthroplasty and trochanteric osteotomy. The Stainless Steel alloy Grip and Grip Plates are intended for use with 2.0mm Stainless Steel beaded and nonbeaded Cables only. Wrought CoCr alloy Grip and Grip Plates are intended for use with 2.0mm CoCr beaded and non-beaded Cables only. Optional Stainless Steel and Titanium screws are also available for use with the Stainless Steel and Wrought CoCr Grip Plates, respectively. #### Indications for Use - The Dall-Miles® System is indicated for reattachment of the trochanter in any hip . procedure using the trochanteric osteotomy (total or partial) approach. - The Dall-Miles® Trochanteric Grips and Grip Plates are indicated for use in the . fixation of the greater trochanter due to trochanteric fracture or osteotomy with intramedullary fixation as the primary device. - The Dall-Miles® Trochanteric Grip Plate is additionally indicated for use in the . fixation of the greater trochanter due to extended trochanteric osteotomies. #### Substantial Equivalence: The Dall-Miles® Trochanteric Grips and Grip Plates are substantially equivalent to the Modified BMP™ Trochanteric Plates, cleared by Biomet (K993510) and the Dall-Miles® Trochanter Cable Super Grip, cleared by Howmedica Osteonics (K962162). {2}------------------------------------------------ #### DEPARTMENT OF HEALTH & HUMAN SERVICES 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 emblem resembling an eagle or bird-like figure with flowing lines, positioned to the right. Encircling the emblem are the words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" in a circular arrangement. #### Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 MAR 0 2 2007 Stryker Orthopaedics % Ms. Patricia Setti-LaPerch Regulatory Affairs Associate 325 Corporate Drive Mahwah, New Jersey 07430 Re: K070170 > Trade/Device Name: Dall-Miles System Regulation Number: 21 CFR 888.3030 Regulation Name: Single/multiple component metallic bone fixation appliances and accessories Regulatory Class: II Product Codes: HRS, LYT, JDQ Dated: January 16, 2007 Received: January 18, 2007 Dear Ms. Setti-LaPerch: 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, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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. {3}------------------------------------------------ #### Page 2 - Ms. Patricia Setti-LaPerch 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); good manufacturing practice requirements as set 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. This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). 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 (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, Mark McMullen Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ 510(k) Number (if known): _K070170 Device Name: Dall-Miles® System ### Indications for Use - The Dall-Miles® System is indicated for reattachment of the trochanter in any hip . procedure using the trochanteric osteotomy (total or partial) approach. - The Dall-Miles® Trochanteric Grips and Grip Plates are indicated for use in the . fixation of the greater trochanter due to trochanteric fracture or osteotomy with intramedullary fixation as the primary device. - The Dall-Miles® Trochanteric Grip Plate is additionally indicated for use in the . fixation of the greater trochanter due to extended trochanteric osteotomies. Prescription Use _____________________________________________________________________________________________________________________________________________________________ Over-the-Counter Use OR (Per 21 CFR 801.109) (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Mark A. Milliken Division of Gener 1, Restorative, and Neurological Devices 510(k) Number K07 0170 --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K070170](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K070170) **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