← Product Code [FMQ](/submissions/HO/subpart-g%E2%80%94general-hospital-and-personal-use-miscellaneous-devices/FMQ) · K971742 # DEPUY ORTHOTECH HEAVY DUTY VEST RESTRAINT (K971742) _Depuy, Inc. · FMQ · Jul 24, 1997 · General Hospital · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/HO/subpart-g%E2%80%94general-hospital-and-personal-use-miscellaneous-devices/FMQ/K971742 ## Device Facts - **Applicant:** Depuy, Inc. - **Product Code:** [FMQ](/submissions/HO/subpart-g%E2%80%94general-hospital-and-personal-use-miscellaneous-devices/FMQ.md) - **Decision Date:** Jul 24, 1997 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 880.6760 - **Device Class:** Class 1 - **Review Panel:** General Hospital ## Indications for Use The DePuy OrthoTech Heavy Duty Vest Restraint is intended to limit body movement and provide support for patients in chairs, wheelchairs and beds who (a) may be susceptible to lifethreatening falls, (b) may be suicidal, or (c) are aggressive. ## Device Story The DePuy OrthoTech Heavy Duty Vest Restraint is a physical restraint device designed to limit patient movement and provide support. It consists of a vest body constructed from three polyester mesh panels (two front, one back) and is equipped with four pairs of long straps for securing the patient to a chair, wheelchair, or bed. The device is available in five sizes (X-small to X-large) to accommodate chest sizes from 28" to 56". It is intended for use in clinical or care settings to manage patients who are aggressive, suicidal, or at risk of life-threatening falls. The device is reusable and can be hand-washed and air-dried. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Constructed from polyester mesh fabric. Consists of three-piece vest design with four pairs of securing straps. Available in five sizes (X-small to X-large). Reusable; hand-washable. ## Regulatory Identification A protective restraint is a device, including but not limited to a wristlet, anklet, vest, mitt, straight jacket, body/limb holder, or other type of strap, that is intended for medical purposes and that limits the patient's movements to the extent necessary for treatment, examination, or protection of the patient or others. ## Predicate Devices - Zimmer Heavy Duty Vest Restraint - DePuy Vest Restraint with Sleeves ([K963393](/device/K963393.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}------------------------------------------------ K971742 ## SAFETY AND EFFECTIVENESS SUMMARY JUL 2 4 1997 | NAME OF FIRM: | DePuy, Inc.
700 Orthopaedic Drive
Warsaw, Indiana 46581-0988
FDA Registration No.: 1818910 | |-----------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------| | FIRM CONTACT: | Arlene Saull, RAC
Manager, Medical Device Submissions
DePuy Orthopaedics, Inc. (a subsidiary of DePuy, Inc.)
700 Orthopaedic Drive
Warsaw, IN 46581-0988 | | TRADE NAME: | DePuy OrthoTech Heavy Duty Vest Restraint | | COMMON NAME: | Protective Restraints | | CLASSIFICATION: | Class I per 21 CFR, 880.6760 Protective Restraint | | DEVICE PRODUCT CODE: | 80 FMQ Restraint, Protective | | SUBSTANTIALLY EQUIVALENT DEVICES: | | SUBSTANTIALLY EQUIVALENT DEVICES Zimmer Heavy Duty Vest Restraint, and DePuy Vest Restraint with Sleeves (K963393) ## DEVICE DESCRIPTION AND INTENDED USE: The body of the vest restraint is constructed from three main pattern pieces, two front panels and a back panel which are cut from polyester mesh fabric. The vest comes equipped with four pairs of long straps which are used for securing the patient to the chair, wheelchair or bed. The subject vest restraint is supplied in five sizes from X-small to X-large to fit chests from 28" to 56". It may be hand washed in warm water and air dried. The DePuy OrthoTech Heavy Duty Vest Restraint is intended to limit body movement and provide support for patients in chairs, wheelchairs and beds who (a) may be susceptible to lifethreatening falls, (b) may be suicidal, or (c) are aggressive .. ## BASIS OF SUBSTANTIAL EQUIVALENCE: Based on their similarities in design, construction, materials, and intended uses, DePuy, Inc. considers the subject DePuy OrthoTech Heavy Duty Vest Restraint as substantially equivalent to the DePuy Mesh Vest Restraint with Sleeves which was cleared by FDA in 510(k) K963393 and the Zimmer Inc. Heavy Duty Vest Restraint. Heavy Duty Vest Restraints {1}------------------------------------------------ Image /page/1/Picture/1 description: The image is a black and white logo for the U.S. Department of Health & Human Services. The logo features a stylized image of three human profiles facing right, with flowing lines beneath them. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged in a circular pattern around the image. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Ms. Arlene C. Saull Manager, Medical Device Submission DePuy, Incorporated_______ 700 Orthopaedic Drive Warsaw, Indiana 46581-0988 JUL 2 4 1997 K971742 Re : DePuy Orthotech Heavy Duty Vest Restraint Trade Name: Regulatory Class: I Product Code: FMQ Dated: May 9, 1997 Received: May 12, 1997 Dear Ms. Saull: 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 concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 {2}------------------------------------------------ Page 2 - Ms. Saull through 542 of the Act for devices under the Electronic enroagle Radiation Control provisions, or other Federal laws or requlations. This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. JThe 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 requlation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4618. 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" (21 CFR 807.97). 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.gov/cdrh/dsmamain.html". Sincerely Yours, A. Ulatowski Time Directbr Division of Dental, Infection Control and General Hospital Devices Office of Device Evaluation Center for Devices and Radioloqical Health Enclosure {3}------------------------------------------------ ## INDICATIONS 510(k) Number (if known)_K971742 Device Name_DePuy OrthoTech Heavy Duty Vest Restraint Indications for Use: ﻤﺴﺘﻤ The DePuy OrthoTech Heavy Duty Vest Restraint is intended to limit body movement and provide support for patients in chairs, wheelchairs and beds who (a) may be susceptible to lifethreatening falls, (b) may be suicidal, or (c) are aggressive. ============================================================================================================================================================================== Concurrence of CDRH, Office of Device Evaluation (Division Sign-Off) Division of Dental. and General Hospit 510(k) Number Prescription Use_ OR Over-the-Counter Use -------(Per 21 CFR 801.109) Heavy Duty Vest Restraints --- **Source:** [https://fda.innolitics.com/submissions/HO/subpart-g%E2%80%94general-hospital-and-personal-use-miscellaneous-devices/FMQ/K971742](https://fda.innolitics.com/submissions/HO/subpart-g%E2%80%94general-hospital-and-personal-use-miscellaneous-devices/FMQ/K971742) **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