GENERAL PRUPOSE LOCALIZERS AND ADAPTERS-NEW ACCESSORIES FOR SONOWAND SYSTEM

K112469 · Sonowand AS · HAW · Mar 23, 2012 · Neurology

Device Facts

Record IDK112469
Device NameGENERAL PRUPOSE LOCALIZERS AND ADAPTERS-NEW ACCESSORIES FOR SONOWAND SYSTEM
ApplicantSonowand AS
Product CodeHAW · Neurology
Decision DateMar 23, 2012
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 882.4560
Device ClassClass 2

Intended Use

The Sonowand Invite System is intended for use as a tool to aid intraoperative ultrasound imaging and image guided surgery during neurosurgery. It is also intended for use as a standard neuronavigation system and as a stand-alone ultrasound scanner. The intended use of a localizer is to enable navigation by showing the position of surgical instruments or pointers relative to MR, CT or Ultrasound images. The General purpose localizers with adapters are intended to be used to attach surgical tools manufactured by other vendors. SonoWand Invite System will display position and orientation of the tools in the medical images on the screen.

Device Story

SonoWand Invite is a neuronavigation system integrating an ultrasound scanner; used in neurosurgery. System tracks position/orientation of surgical tools or pointers relative to MR, CT, or ultrasound images. New accessories (general purpose localizers and adapters) allow attachment of third-party surgical tools to the system. Surgeon operates system via graphical touch screen or footswitch. Output displayed on screen; assists surgeon in visualizing tool location relative to patient anatomy during procedures. Benefits include improved navigation accuracy and intraoperative imaging capabilities.

Clinical Evidence

Bench testing only. No clinical data. Testing included cleaning and sterilization validation, system integration testing, and verification of fit, calibration, and accuracy for the new localizers and adapters.

Technological Characteristics

Materials: 316L Stainless steel, 6082 Aluminium with DLC coating, and Radel PPSU (PEEK). System integrates ultrasound scanner with neuronavigation rack. Connectivity: Touch screen and footswitch interface. Sterilization: Compatible with standard surgical cleaning/sterilization protocols. Biocompatibility: Compliant with USP and ISO 10993-1.

Indications for Use

Indicated for neurosurgery patients requiring intraoperative ultrasound imaging or image-guided surgery. Used by surgeons to track surgical instruments or pointers relative to preoperative MR, CT, or intraoperative ultrasound images.

Regulatory Classification

Identification

A stereotaxic instrument is a device consisting of a rigid frame with a calibrated guide mechanism for precisely positioning probes or other devices within a patient's brain, spinal cord, or other part of the nervous system.

Predicate Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ 510(k) Summarv KII 2469 t 510(k) Number: | Device Trade Name: | General purpose localizers and adapters - new accessories for SonoWand Invite System | |-------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------| | Device Common Name: | Diagnostic ultrasound neuronavigation intraoperative imaging system | | Device Regulation Name: | Sterotaxic instrument (21 CFR 882.4560, Class II, Code: HAW,IYN) | | Submitter: | SONOWAND AS<br>Nedre lla 39<br>7018 Trondheim<br>NORWAY<br>Phone number: 0047 73805900 | | Contact Information: | Constance G. Bundy<br>C. G. Bundy Associates, Inc.<br>435 Rice Creek Terrace NE<br>Fridley, MN 55432<br>763-574-1976<br>Fax: 763-571-2437<br>cgbundy@live.com | | Submission Date: | August 24, 2011 | ## Equivalent Device Identification: The purpose of this submission is to add additional accessories to the SonoWand Invite System. The additional accessories are general purpose localizers with adapters. These accessories are equivalent in function and intended use to the Navigator tool which was cleared in the original 510(k), K083597. ### Device Description: The 510(k) cleared SonoWand Invite System is a neuronavigation system with intraoperative imaging capabilities. An ultrasound scanner is physically integrated with a neuronavigation system in a single rack of equipment. SonoWand Invite can be used as a conventional neuronavigation system based on preoperative MR or CT-images, or as a stand-alone ultrasound scanner for real-time 2D imaging or as a combined system where 3D ultrasound data can be transferred to the navigation system for direct navigation. SonoWand Invite has basically two functionalities. It supports the surgeon by showing the position of tools or pointers relative to MR, CT or Ultrasound images. It also makes it possible for the surgeon to acquire ultrasound images during operation, which can be compared with other images (such as MR or CT) and can be used for supporting the surgeon by showing the position of tools and pointers. The control is primarily by a graphical touch screen. The secondary control is by a footswitch. The new accessories, General purpose localizers with adapters, shall be used to attach surgical tools manufactured by other vendors. SonoWand Invite will then display position and orientation of the tools in the medical images on the screen in the same way as the previous 510(k) cleared Navigator tool. The localizers with adapters are designed to fit surgical tools normally used in the operating room. There are no changes to the Intended use, function or technological aspects including software of the SonoWand Invite. The additional accessories are being added to increase usability of the SonoWand Invite system. {1}------------------------------------------------ K112469 ## Intended Use: The Sonowand Invite system is intended for use as a tool to aid intraoperative ultrasound imaging and image guided surgery during neurosurgery. It is also intended for use as a standard neuronavigation system and as a stand-alone ultrasound scanner. The intended use of a localizer is to enable navigation by showing the position of surgical instruments or pointers relative to MR, CT or Ultrasound images The General purpose localizers with adapters are intended to be used to attach surgical tools manufactured by other vendors. SonoWand Invite System will display position and orientation of the tools in the medical images on the screen. ## Comparison Chart: | Element of<br>Comparison | Subject | Predicate Device | Comment | | | |-----------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | SonoWand Invite new<br>accessories | K083597<br>SonoWand Invite<br>accessories | | | | | Common<br>name | General<br>purpose<br>localizers,<br>small and<br>large | User tool<br>adapters (*)<br>Bracket &<br>Clamp adapter | Navigator,<br>intraoperative | Probe<br>localizers<br>for variable<br>size<br>ultrasound<br>probes | | | Pictures | Image: General purpose localizers | Image: User tool adapters | Image: Navigator | Image: Probe localizers | Accessories are<br>biocompatible and<br>sterilizable. | | | Image: General purpose localizers | Image: User tool adapters | Image: Navigator | Image: Probe localizers | | | Intended<br>use of<br>accessories | The intended<br>use of a<br>localizer is to<br>enable<br>navigation by<br>showing the<br>position of<br>surgical<br>instruments or<br>pointers relative<br>to MR, CT or<br>Ultrasound<br>images | The adapter is<br>intended to<br>connect the<br>general purpose<br>localizer with a<br>variety of<br>surgical<br>instruments | The intended use<br>of a localizer is to<br>enable navigation<br>by showing the<br>position of the<br>Navigator (pointer)<br>relative to MR, CT<br>or Ultrasound<br>images | The intended<br>use of a probe<br>localizer is to<br>enable<br>accurate<br>imaging during<br>surgery by<br>tracking the<br>probes<br>location<br>relative to the<br>patient. | No changes to<br>intended use or the<br>functionality of<br>SonoWand Invite(**).<br>The adapted surgical<br>instruments are given<br>the same functionality<br>as the Navigator<br>(pointer).<br>Connecting a localizer<br>to the device does not<br>affect the intended use<br>of the connected<br>device. | | Materials | 316 L Stainless<br>steel,<br>6082 Aluminium<br>DLC Coating | 316 L Stainless<br>steel,<br>Plastic Radel<br>PPSU (PEEK) | 316 L Stainless<br>steel,<br>6082 Aluminium<br>DLC Coating | 316 L<br>Stainless<br>steel,<br>6082<br>Aluminium<br>DLC Coating | New material; Plastic<br>Radel PPSU (PEEK)<br>are widely used for<br>surgical instruments.<br>The material is in<br>compliance with both<br>United States<br>Pharmacopeias (USP)<br>and ISO 10993-1<br>guideline requirements<br>for Biocompatibility<br>Testing of Materials. | {2}------------------------------------------------ K112469 (*) Images show adapters attached to localizers (**) SonoWand Invite has basically two functionalities. It supports the surgeon by showing the position of tools or pointers relative to MR, CT or Ultrasound images. It also makes it possible for the surgeon to acquire ultrasound images during operation, which can be compared with other images (such as MR or CT) and can be used for surgeon by showing the position of tools and pointers. #### Intended use: There are no changes to the Intended use of the SonoWand Invite. The additional accessories (localizers and adapters) will facilitate the commonly used surgical instruments with the same functionality as the Navigator (pointer). Connecting a localizer to the device does not affect the intended use of the connected device. #### Technological and performance characteristics: Technological characteristics of the localizers and adapters, including device design and performance, are substantially equivalent to the accessories of the predicate device SonoWand Invite. K083597. #### Summary of Testing: The new localizers and adapters have been tested to and comply with all applicable cleaning and sterilization standards. The devices subject to this submission do not contain software module in the cleared SonoWand Invite System that supports the function of the subject devices has been tested to and complies with requirements. The Localizers have been tested to and comply with requirements of the SonoWand Invite System Test. The Adapters were tested for fit, calibration and accuracy. Results of the tests performed show the General purpose localizers and adapters are as safe and effective as the accessories of the predicate device. #### Conclusion: The conclusion drawn from the testing is that the localizers and adapters can be used for supporting the surgeon by showing the position of surgical tools. Connecting a localizer to the device does not affect the intended use of the connected device. Results of the tests performed show the new accessories (localizers and adapters) to SonoWand Invite are as safe and effective as the predicate devices. {3}------------------------------------------------ ## DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three overlapping wings, representing the department's commitment to health, human services, and well-being. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged in a circular fashion around the eagle symbol. #### Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002 Sonowand AS % C.G. Bundy Associates, Inc. Ms. Constance G. Bundy 435 Rice Creek Terrace NE Fridley, Minnesota 55432 Re: K112469 Trade/Device Name: General purpose localizers and adapters - new accessories for SonoWand Invite System Regulation Number: 21 CFR 882.4560 Regulation Name: Stereotaxic instrument Regulatory Class: II Product Code: HAW, IYN Dated: March 14, 2012 Received: March 20, 2012 Dear Ms. Bundy: 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. 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 MAR 2 3 2012 {4}------------------------------------------------ Page 2 - Ms. Constance G. Bundy 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 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/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 yours, Erinl Keith Mark N. Melkerson Director Division of Surgical, Orthopedic and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ ## wand # Indications for Use K112469 510(k) Number (if known): Device Name: General purpose localizers and adapters - new accessories for SonoWand Invite System Indications For Use: The Sonowand Invite System is intended for use as a tool to aid intraoperative ultrasound imaging and image guided surgery during neurosurgery. It is also intended for use as a standard neuronavigation system and as a stand-alone ultrasound scanner. The intended use of a localizer is to enable navigation by showing the position of surgical instruments or pointers relative to MR, CT or Ultrasound images The General purpose localizers with adapters are intended to be used to attach surgical tools manufactured by other vendors. SonoWand Invite System will display position and orientation of the tools in the medical images on the screen. Prescription Use (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Neil R.P. Ogle for mx (Division Sign-Off) Division of Surgical, Orthopedic, and Restorative Devices 510(k) Number K112469
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