← Product Code [HRS](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS) · K973982 # ORBITAL RECONSTRUCTION PLATES (K973982) _Howmedica, Inc. · HRS · Jan 12, 1998 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K973982 ## Device Facts - **Applicant:** Howmedica, Inc. - **Product Code:** [HRS](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS.md) - **Decision Date:** Jan 12, 1998 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3030 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use The plates are intended for use in patients requiring craniofacial reconstruction of the internal orbit. These plates provide structure and support to the orbital walls and/or floor when anatomical reconstruction of the internal orbit is necessary. ## Device Story Orbital Reconstruction Plates are titanium plates of varying configurations and thicknesses; designed to provide structural support to internal orbital walls and/or floor during craniofacial reconstruction. Used by surgeons in clinical settings to accommodate specific patient anatomy and extent of reconstruction required. Plates are secured using previously cleared screws. Device provides mechanical stabilization of orbital defects; facilitating anatomical reconstruction. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Titanium bone plates; varying configurations and thicknesses; mechanical fixation; non-powered; non-implantable software. ## 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 - TiMesh's Titanium Mesh Tilghman Orbit Liner - Synthes' Universal Orbital Floor Plate ## 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}------------------------------------------------ K973982 ## 510(k) Summary July 12 1998 | Proprietary Name: | Orbital Reconstruction Plates | |----------------------------|--------------------------------------------------| | Common Name: | Bone Plates | | Classification Name | Single/Multiple Component Metallic Bone Fixation | | Reference: | Appliances and Accessories (21 CFR 888.3030) | | Proposed Regulatory Class: | II | | Device Product Code: | 87HRS | Vivian Kelly For information contact: Manager, Regulatory Affairs Howmedica Inc. 359 Veterans Boulevard Rutherford, NJ 07070 Telephone: (201) 507-7830 Fax: (201) 507-6870 The Orbital Reconstruction Plates are a series of plates made from titanium with different configurations and thicknesses. The configurations vary to accommodate the level of reconstruction required or the patient's anatomy. The difference in thickness provides the necessary support for the internal orbit based on the type and extent of reconstruction required. The screws used with plates were previously cleared under various premarket notifications. The plates are intended for use in patients requiring craniofacial reconstruction of the internal orbit. These plates provide structure and support to the orbital walls and/or floor when anatomical reconstruction of the internal orbit is necessary. The substantial equivalence of these components is based on an equivalence in intended use, materials, design, and operational principles to other predicate devices used for orbital reconstruction plates such TiMesh's Titanium Mesh Tilghman Orbit Liner and Synthes' Universal Orbital Floor Plate. {1}------------------------------------------------ Image /page/1/Picture/2 description: The image is a black and white logo for the U.S. Department of Health & Human Services. The logo features the department's name in a circular arrangement around a stylized emblem. The emblem consists of a symbol that resembles a stylized caduceus, with three abstract shapes that could be interpreted as wings or flowing lines. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 JAN 1 2 1998 Ms. Vivian Kelly · Manager, Regulatory Affairs Howmedica Inc. Pfizer Hospital Products Group 359 Veterans Boulevard Rutherford, New Jersey 07070-2584 Re: K973982 Orbital Reconstruction Plates Trade Name: Regulatory Class: II Product Code: HRS Dated: October 16, 1997 Received: October 20, 1997 Dear Ms. Kelly: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act 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 (Premarket Approval), 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 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (QS) for Medical Devices: General requlation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements Please note: concerning your device in the Federal Register. this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or requlations. {2}------------------------------------------------ Page 2 - Ms. Vivian Kelly This letter will allow you to begin marketing your device as described in your 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 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 ene rogalacion Chercross, "Mobianany" (2) Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.qov/cdrh/dsmamain.html". Sincerely yours, Calvin M. Whittier, Ph.D., M. -Celia M. Witten, Ph.D., M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ ## Indications for Use 510(k) Number (if known): |<973982 Device Name: Orbital Reconstruction Plates Indications for Use: The plates are intended for use in patients requiring craniofacial reconstruction of the internal orbit. These plates provide structure and support to the orbit walls and/or floor when anatomical reconstruction of the internal orbit is necessary. (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) | Prescription Use (Per 21 CFR 801.109) |
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OR Over-The-Counter Use ______ | |---------------------------------------|-----------------------------------------------------------------------------------------------| |---------------------------------------|-----------------------------------------------------------------------------------------------| (Optional Format 1-2-96) (Division Sign-Off) Division of General Restorative Devices | 510(k) Number | K973902 | |---------------|---------| |---------------|---------| --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K973982](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K973982) **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