← Product Code [HRS](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS) · K012114 # SYNTHES LOCKING DISTAL RADIUS PLATING SYSTEM (K012114) _Synthes (Usa) · HRS · Sep 28, 2001 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K012114 ## Device Facts - **Applicant:** Synthes (Usa) - **Product Code:** [HRS](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS.md) - **Decision Date:** Sep 28, 2001 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3030 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use The Synthes Locking Distal Radius Plating System is intended for fixation of complex intra- and extra-articular fractures and osteotomies of the distal radius and other small bones. ## Device Story The Synthes Locking Distal Radius Plating System consists of machined metallic plates and screws designed for internal fixation of bone fractures. The system provides a locking mechanism between the screw and the plate to enhance stability. It is intended for use by surgeons in an operating room setting to treat complex intra- and extra-articular fractures and osteotomies of the distal radius and other small bones. The device is implanted to provide rigid fixation, facilitating bone healing and restoring anatomical alignment. It serves as a mechanical support system for orthopedic procedures. ## Clinical Evidence bench testing only ## Technological Characteristics Materials: Stainless steel or titanium plates and screws. Design: Machined metallic plates with screw-to-plate locking mechanism. Energy source: None (mechanical device). Sterilization: Not specified. ## 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 - Synthes Distal Radius Plate System ## 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}------------------------------------------------ K012114 : 上一 # SEP 2 8 2001 #### Summary of Safety and Effectiveness Information 3. | Sponsor | Synthes (USA)
1690 Russell Road
Paoli, PA 19301 | |--------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Company Contact | Matthew M. Hull
(610) 647-9700 ext. 7191 | | Name of the Device | Synthes Locking Distal Radius Plating System | | Device Classification(s) | Class II, §888.3030 - Plate, Fixation, Bone
Class II, §888.3040 - Screw, Fixation, Bone | | Predicate Device | - Synthes Distal Radius Plate System | | Device Description | The Synthes Locking Distal Radius Plating System consists of
machined metallic plates and screws that offer screw to plate locking
designed for various fracture modes of the distal end of the radius. | | Indications | The Synthes Locking Distal Radius Plating System is intended for
fixation of complex intra- and extra-articular fractures and
osteotomies of the distal radius and other small bones. | | Materials | Plates: Stainless Steel or Titanium
Screws: Titanium or Stainless Steel | : · . 00005 : {1}------------------------------------------------ Image /page/1/Picture/1 description: The image shows the seal of the U.S. Department of Health and Human Services. The seal features a stylized caduceus, a symbol often associated with medicine and healthcare, with a bird-like design. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged in a circular pattern around the symbol. The seal is black and white. SEP 2 8 2001 Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Mr. Matthew M. Hull, RAC Senior Regulatory Specialist Synthes, USA 1690 Russell Road P. O. Box 1766 Paoli, Pennsylvania 19301 Re: K012114 Trade/Device Name: Synthes Locking Distal Radius Plating System Regulation Number: 888.3030, 888.3040 Regulation Name: Plate, fixation, bone Screw, fixation, bone Regulatory Class: II Product Code: HRS, HWC Dated: July 5, 2001 Received: July 6, 2001 Dear Mr. Hull: We have reviewed your Section 510(k) premarket notification of intent to market the device we nave roviewed your betermined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate 10. use stated in the encreated) 7. the enactment date of the Medical Device Amendments, or to conniner of prior to 110) 2011-11-11 in accordance with the provisions of the Federal Food, Drug, do noos that have been that do not require approval of a premarket approval application (PMA). and Cosmeter for (110) and the device, subject to the general controls provisions of the Act. The I ou may , and second 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 If your device 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. 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 Orth 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. {2}------------------------------------------------ ### Page 2 - Mr. Matthew M. Hull, RAC 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 and additionally 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4659. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Ouvision of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html Sincerely yours, sincerely yours, Mark N. Melberse Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ K012114 #### Indications for Use Statement 2. 510(k) Number (if known): ## KOLAI14 ______________________________________________________________________________________________________________________________________________________________________ Device Name: Indications for Use: Synthes Locking Distal Radius Plating System The Synthes Locking Distal Radius Plating System is intended for fixation of complex intra- and extraarticular fractures and osteotomies of the distal radius and other small bones. (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) # Concurrence of CDRH, Office of Device Evaluation (ODE) | Prescription Use | OR | Over-The-Counter Use_ | |----------------------|----|-----------------------| | (Per 21 CFR 801.109) | | | ![signature](signature.png) | | (Division Sign-Off) | |--|-----------------------------------------------------------| | | Division of General, Restorative and Neurological Devices | K012114 510(k) Number - CONFIDENTIAL Synthes(USA) Synthes Locking Distal Radius Plating System 510(k) ### 000004 --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K012114](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K012114) **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. 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