The Stryker Precision HD Camera System is indicated for use in general laparoscopy, nasopharyngoscopy, ear endoscopy, sinuscopy, and plastic surgery wherever a laparoscope/endoscope/arthroscope is indicated for use.

A few examples of the more common endoscopic surgeries are listed below.

· laparoscopic cholecystectomy
· laparoscopic hernia repair
· laparoscopic appendectomy
laparoscopic pelvic lymph node dissection
· laparoscopically assisted hysterectomy
· laparoscopic and thorascopic anterior spinal fusion
anterior cruciate ligament reconstruction
· knee arthroscopy
· shoulder arthroscopy
small joint arthroscopy
· decompression fixation
· wedge resection
· lung biopsy
· pleural biopsy
dorsal sympathectomy
· pleurodesis
· internal mammary artery dissection for coronary artery bypass
coronary artery bypass grafting where endoscopic visualization is indicated
· examination of the evacuated cardiac chamber during performance of valve replacement

The users of the camera are general surgeons, gynecologists, cardiac surgeons, plastic surgeons, orthopedic surgeons, ENT surgeons and urologists.

Device Description

The Stryker Precision HD Camera Systems (hereafter referred to as "proposed device") is an endoscopic camera system that is used together with an endoscope to view endoscopic surgical sites on video monitors. The system consists of a Camera Control Unit (CCU), a Coupler, and a Camera Head with an integral cable that connects to the CCU. The optical image is transferred from the surgical site to the camera head by a variety of rigid and flexible scopes that are attached to the camera head using an optical coupler or by direct connection. Sterilization of the Coupler and Camera Head is required before use. The Coupler and Camera Head can be sterilized using steam sterilization.

AI/ML Overview

The provided text describes a 510(k) submission for the Stryker Precision HD Camera System, which is a medical device for endoscopic visualization in various surgical procedures. Unfortunately, the document does not contain an "acceptance criteria" table with specific device performance metrics in numerical form.

Instead, the document focuses on demonstrating substantial equivalence to a predicate device (Stryker 1488 HD Video Camera with Infrared Compatibility) by highlighting similar technological characteristics and adherence to various safety and performance standards. The "Performance Data" section describes the types of tests conducted but does not provide quantitative results or specific acceptance criteria for those tests.

Therefore, many of the requested details, such as specific performance metrics and their acceptance criteria, sample sizes for test and training sets, details about ground truth establishment, or information about MRMC studies, are not present in this 510(k) summary.

However, I can extract the following information that is available in the text:

1. Table of Acceptance Criteria and Reported Device Performance:

As mentioned, a specific table with numerical acceptance criteria and reported device performance is not included in this document. The document states that "Bench performance testing was conducted to ensure that the device functioned as intended and met design specifications and acceptance criteria." However, it does not detail what those specific criteria or the measured performance values were. It primarily focuses on compliance with standards.

2. Sample Size Used for the Test Set and Data Provenance:

Sample Size for Test Set: Not specified. The document mentions "Bench performance testing" and compliance with standards but does not provide a specific sample size for a test set of data. This submission is for a camera system, not for an AI algorithm or a diagnostic device that processes specific patient data for a diagnostic outcome.
Data Provenance: Not applicable in the context of an AI device's test set. The performance testing described relates to the camera's hardware and software functionality and compliance with electrical, EMC, and sterilization standards.

3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications:

Not applicable. This document describes a camera system for visualization, not a diagnostic device that requires expert-established ground truth on medical images or data for performance evaluation. The "truth" in this context would be the camera's ability to accurately capture and display images, which is assessed through technical performance testing, not expert interpretation of medical cases.

4. Adjudication Method for the Test Set:

Not applicable. See point 3. Adjudication methods are typically used for diagnostic studies involving human interpretation or AI outputs, not for the functional testing of a camera system.

5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study was done:

No. An MRMC study was not done or described. This type of study is relevant for evaluating the impact of an AI system on human reader performance, which is not the scope of this device's submission as presented.

6. If a Standalone (i.e., algorithm only without human-in-the-loop performance) was done:

Not applicable. This device is a camera system, and while it contains software, its primary function is to provide visual input to a human surgeon. It is not an "algorithm only" device in the sense of an AI diagnostic tool. Its performance is intrinsically linked to its use in a human-in-the-loop context during surgery.

7. The Type of Ground Truth Used:

Technical Specifications/Standards. For this type of device (a camera system), the "ground truth" used for testing would be compliance with established engineering design specifications, performance standards (e.g., image resolution, color accuracy, electrical safety, electromagnetic compatibility), and successful sterilization validation. It does not involve medical ground truth like pathology or outcomes data in the way an AI diagnostic tool would.

8. The Sample Size for the Training Set:

Not applicable / Not specified. This document does not describe an AI system that undergoes training on a dataset of medical cases. The software mentioned is for controlling the camera system (e.g., user interface, surgical mode selections), not for an AI model trained on data for diagnostic or assistive tasks.

9. How the Ground Truth for the Training Set was Established:

Not applicable / Not described. See point 8. There is no mention of a training set or corresponding ground truth establishment for an AI algorithm.

Summary

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Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is an abstract image of a stylized eagle or bird with three human profiles incorporated into its design.

Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

October 23, 2014

Stryker Endoscopy Mr. Dave Yungvirt Third Party Review Group, LLC 45 Rockefeller Plaza, Suite 2000 New York, New York 10111

Re: K142603

Trade/Device Name: Stryker Precision HD Camera System Regulation Number: 21 CFR 876.1500 Regulation Name: Endoscope and accessories Regulatory Class: Class II Product Code: GJC Dated: October 9, 2014 Received: October 10, 2014

Dear Ms. Yungvirt:

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 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); medical device reporting (reporting of medical

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device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (OS) 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 contact the Division of Industry and Consumer Education 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. 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 Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely yours.

David Krause -S

for

Binita S. Ashar, M.D., M.B.A., F.A.C.S. Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Indications for Use

510(k) Number (if known) K142603

Device Name

Stryker Precision HD Camera System

Indications for Use (Describe)

A few examples of the more common endoscopic surgeries are listed below.

· laparoscopic cholecystectomy
· laparoscopic hernia repair
· laparoscopic appendectomy
laparoscopic pelvic lymph node dissection
· laparoscopically assisted hysterectomy
· laparoscopic and thorascopic anterior spinal fusion
anterior cruciate ligament reconstruction
· knee arthroscopy
· shoulder arthroscopy
small joint arthroscopy
· decompression fixation
· wedge resection
· lung biopsy
· pleural biopsy
dorsal sympathectomy
· pleurodesis
· internal mammary artery dissection for coronary artery bypass
coronary artery bypass grafting where endoscopic visualization is indicated
· examination of the evacuated cardiac chamber during performance of valve replacement

The users of the camera are general surgeons, gynecologists, cardiac surgeons, plastic surgeons, orthopedic surgeons, ENT surgeons and urologists.

Type of Use (Select one or both, as applicable)

2 Prescription Use (Part 21 CFR 801 Subpart D)

Over-The-Counter Use (21 CFR 801 Subpart C)

PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED.

FOR FDA USE ONLY

Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)

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Image /page/3/Picture/1 description: The image shows the Stryker logo in black and white. The logo is a stylized wordmark with a bold, sans-serif font. The registered trademark symbol is located to the right of the word "Stryker".

510(k) SUMMARY

1) General Information

510(k) Sponsor	Stryker Endoscopy
Address	5900 Optical CourtSan Jose, CA 95138
FDA Registration Number	2936485
Correspondence Person	Angela WongStaff Regulatory Affairs AnalystStryker Endoscopy
Contact Information	Email: angela.wong @ stryker.comPhone: (408) 754-2737
Date Prepared	10 September 2014

2) Proposed Device

Proprietary Name	Stryker Precision HD Camera System
Common Name	3-Chip Video Camera
Classification Name	Laparoscope, General and Plastic Surgery
Regulation Number	21 CFR 876.1500
Product Code	GCJ
Regulatory Class	II

3) Predicate Device

Proprietary Name	Stryker 1488 HD Video Camera with Infrared Compatibility
Common Name	3-Chip Video Camera
Premarket Notification	K132785
Classification Name	Laparoscope, General and Plastic Surgery
Regulation Number	21 CFR 876.1500
Product Code	GCJ
Regulatory Class	II

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4) Device Description

ട്) Indication for Use

A few examples of the more common endoscopic surgeries are listed below.

laparoscopic cholecystectomy
laparoscopic hernia repair
laparoscopic appendectomy ●
. laparoscopic pelvic lymph node dissection
laparoscopically assisted hysterectomy
laparoscopic and thorascopic anterior spinal fusion ●
anterior cruciate ligament reconstruction
knee arthroscopy
shoulder arthroscopy
small joint arthroscopy
decompression fixation
wedge resection
lung biopsy
pleural biopsy
dorsal sympathectomy ●
pleurodesis
internal mammary artery dissection for coronary artery bypass
coronary artery bypass grafting where endoscopic visualization is indicated ●
examination of the evacuated cardiac chamber during performance of valve ● replacement

The users of the camera are general surgeons, gynecologists, cardiac surgeons, thoracic surgeons, plastic surgeons, orthopedic surgeons, ENT surgeons and urologists.

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Stryker® Precision HD Camera System. 510(k) Summary

6) Comparison of Technological Characteristics with the Predicate Device

The Stryker Precision HD Camera System has the same technological characteristics and design as the predicate device except the following features:

a) A change in sterilization method Uses steam sterilization method
b) A change in sensor technology within the camera head Uses Charge-coupled device (CCD) sensor
c) Modification to the surgical mode selection on the CCU's interface touchscreen -It should be noted that the Stryker Precision HD Camera System does not include "Infrared" surgical mode selection on its interface touchscreen but it is sensitive to Infrared band. The proposed device maintains its Infrared capability by displaying the Infrared light as red image when used with Stryker Infravision Illuminator.

All other technological characteristics of both proposed and predicate devices are identical. Both devices consist of three main components: a camera head, a coupler, and a Camera Control Unit (CCU). Both devices receive optical image from a variety of scopes that are attached to the camera head via coupler and use image sensor to convert optical image into electronic signal. Both camera heads feature a button keypad for controlling of the device itself and the connected video peripheral devices. Both camera systems are sensitive to specific IR band.

The Camera Control Unit (CCU) of both devices contains software and acts as the control center of the device. The CCU of both devices contains a touchscreen with graphical user interface (GUI). The touchscreen menu of both devices has pre-defined surgical mode selections menu to allow users to optimize camera setting base on different surgical specialties.

The CCU of both devices is not intended to enter the sterile field, and should not be sterilized. The camera head and coupler of both devices are reusable devices and shall be sterilized prior to the first use and after every subsequent use.

7) Performance Data

The Precision HD Camera System was tested for performance in accordance with internal design specification and with the applicable performance standards.

Electrical safety and electromagnetic compatibility testing was performed in accordance to the standards listed below. Testing indicates that the proposed device conforms to these standards.

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Stryker® Precision HD Camera System. 510(k) Summary

. ANSI/AAMI ES60601-1:2005+A2 (R2012) + A1- Medical Electrical Equipment – Part 1: General Requirements for Basic Safety and Essential Performance
. IEC60601-1-2:2007 - Medical Electrical Equipment – Part 1-2: General Requirements for Basic Safety and Essential Performance – Collateral Standard: Electromagnetic Compatibility - Requirements and Tests,
IEC60601-2-18:2009 Medical Electrical Equipment Part 2-18: Particular ● Requirements for the Basic Safety and Essential Performance of Endoscopic Equipment

Software was developed, tested, and verified per FDA guidance documents, "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices" and IEC 62304:2006 - Medical Device Software - Software Life Cycle Processes. The software for this device was considered as a "moderate" level of concern, since a failure or latent flaw in the software could result in minor injury to the patient or operator.

The cleaning instructions provided in the labeling for reusable components were validated. Sterilization validation testing activities were performed in accordance with ISO 14937:2009- Sterilization of Health Care Products — General Requirements for Characterization of a Sterilizing Agent and the Development. Validation and Routine Control of a Sterilization Process for Medical Devices.

Bench performance testing was conducted to ensure that the device functioned as intended and met design specifications and acceptance criteria. Bench testing included video compatibility, DVI compliance, and system compatibility. Test results obtained verified the safety and effectiveness of the devices per design specifications and applicable standards.

8) Conclusion

Base on the indication of use, technological characteristic, performance testing and comparison to the predicate device, the Stryker Precision HD Camera System raises no new questions of safety and effectiveness as compared to the predicate device and is substantially equivalent to the predicate devices in terms of safety, efficacy and performance.

Regulation Number and Section

§ 876.1500 Endoscope and accessories.

(a)
Identification. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.(b)
Classification —(1)Class II (special controls). The device, when it is an endoscope disinfectant basin, which consists solely of a container that holds disinfectant and endoscopes and accessories; an endoscopic magnetic retriever intended for single use; sterile scissors for cystoscope intended for single use; a disposable, non-powered endoscopic grasping/cutting instrument intended for single use; a diagnostic incandescent light source; a fiberoptic photographic light source; a routine fiberoptic light source; an endoscopic sponge carrier; a xenon arc endoscope light source; an endoscope transformer; an LED light source; or a gastroenterology-urology endoscopic guidewire, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I for the photographic accessories for endoscope, miscellaneous bulb adapter for endoscope, binocular attachment for endoscope, eyepiece attachment for prescription lens, teaching attachment, inflation bulb, measuring device for panendoscope, photographic equipment for physiologic function monitor, special lens instrument for endoscope, smoke removal tube, rechargeable battery box, pocket battery box, bite block for endoscope, and cleaning brush for endoscope. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807of this chapter, subject to the limitations in § 876.9.