(87 days)
Not Found
No
The summary describes a computer-assisted surgical guidance system using optical tracking and pre-operative imaging. There is no mention of AI, ML, or related concepts in the device description, intended use, or performance studies.
No.
The device is an intraoperative guidance system used during surgery, assisting in instrument positioning and locating anatomical structures, rather than directly treating a medical condition or restoring function.
No
The Stryker Q Guidance System is an intraoperative guidance system that assists surgeons in positioning instruments and locating patient anatomy during surgery. It is not intended for diagnostic purposes, such as identifying or characterizing a disease or condition.
No
The device description explicitly states that the system is comprised of a computer platform, navigated accessories/instruments (e.g., patient/instrument trackers, pointers), and various system components (i.e. Calibration Body, Registration Pointer, etc.), in addition to the software. This indicates the presence of significant hardware components beyond just a general-purpose computing platform.
Based on the provided information, the Stryker Q Guidance System is not an IVD (In Vitro Diagnostic) device.
Here's why:
- Intended Use: The intended use clearly states that the system is a "planning and intraoperative guidance system to enable open or percutaneous computer assisted surgery." It assists in the positioning of instruments and locating anatomical structures during surgical procedures.
- Device Description: The description details a system comprised of computer hardware, software, navigated accessories, and tracking technology used to guide surgical instruments relative to patient images.
- Lack of In Vitro Activities: There is no mention of the device being used to examine specimens (like blood, tissue, or urine) outside of the body to provide information for diagnosis, monitoring, or treatment. IVD devices are specifically designed for these types of tests.
- Focus on Surgical Guidance: The entire description and performance data revolve around the accuracy and functionality of the system in guiding surgical procedures and instruments within the patient's body.
In summary, the Stryker Q Guidance System is a surgical navigation and guidance system, not a device used for in vitro diagnostic testing.
N/A
Intended Use / Indications for Use
The Stryker Q Guidance System, when used with the Spine Guidance software, is intended as a planning and intraoperative guidance system to enable open or percutaneous computer assisted surgery in adult and pediatric (adolescent) patients.
The system is indicated for any surgical procedure on the spine in which the use of computer assisted planning and surgery may be appropriate. The system can be used for intraoperative guidance where a reference to a rigid anatomical structure such as the spine, pelvis or skull can be identified.
The system assists in the positioning of instruments for procedures on the spine and pelvis, including:
- Screw Placement in the spine or pelvis
The Q Guidance System is intended as an aid for precisely locating anatomical structures in open or percutaneous computer assisted surgery. The system is indicated for any medical condition in which the use of computer assisted planning and surgery may be appropriate and where reference to a rigid anatomical structure such as the skull, vertebra, or long bone can be identified.
Product codes (comma separated list FDA assigned to the subject device)
OLO
Device Description
The Stryker Q Guidance System with Spine Guidance 4.0 Software system is a computer-assisted stereotaxic, image-guided, planning, and intraoperative guidance system intended to enable open or percutaneous computer-assisted surgery. It assists the surgeon in precisely positioning instruments and locating patient anatomy during spinal surgery.
The Q Guidance System with Spine Guidance 4.0 Software system is comprised of a computer platform, Spine Guidance Software, navigated accessories/ instruments (e.g., patient/ instrument trackers, pointers), and various system components (i.e. Calibration Body, Registration Pointer, etc.). The system provides intraoperative guidance to the surgeon using passive and active wireless optical tracking technologies. The computer platform consists of a computer, camera, big touchscreen monitor, and a small touchscreen monitor.
The Spine Guidance 4.0 Software is dedicated to spine surgical procedures as defined in the indications for use. Required navigated instruments include a patient tracker, an instrument tracker, pointers, etc. An instrument battery is required when a battery powered instrument or calibration device is used.
The Spine Guidance 4.0 Software displays the intraoperative location of navigated surgical instruments relative to imported patient medical images via wireless optical tracking technology. The software provides the functions to perform the indicated navigated spine surgical procedures. The software guides the user through the necessary preoperative and intraoperative steps required to set-up and perform the navigated spine surgical procedures.
The Spine Guidance 4.0 Software system includes the system components described below.
- Flat Disc Stick-On Fiducials A
The Flat Disc Stick-On Fiducials are passive imaging device trackers designed specifically for use with the AIRO Mobile TruCT System. The Flat Disc Stick-On Fiducials combine to form a passive tracker used for automatically registering patient image data with the patient tracker in place. - A Calibration Body
The Calibration Body is used to validate and calibrate active and passive optically navigated instruments when used with the Spine Guidance Software system. - A Registration Pointer
The Registration Pointers are optional accessories to the Spine Guidance Software. They include pins for the connection of reflective spheres that allow them to be tracked by the Spine Guidance Software system. - A Mayfield Base with Articulating Arm
The Mayfield Base with Articulating Arm has a mechanical interface to the starburst connection on skull clamps. A Universal Tracker or an nGenius Universal Tracker can be attached to the Mayfield Base with Articulating Arm to enable tracking by the Spine Guidance Software system.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
- Computed tomography (CT)
- Computed tomography angiography (CTA)
- Magnetic resonance (MR)
- Magnetic resonance angiography (MRA)
- Position emission tomography (PET)
Anatomical Site
Spine, pelvis, skull, vertebra, long bone
Indicated Patient Age Range
Adult and pediatric (adolescent) patients
Intended User / Care Setting
Operating Room (OR)
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
The function and performance of the subject devices (i.e., Stryker Q Guidance System with Spine Guidance Software (including the system components listed above) have been evaluated through non-clinical design verification and validation testing. The results of the evaluation tests demonstrate that the subject devices successfully meet the requirements of their intended use.
Additional testing was performed on the subject devices to ensure they met their design requirements.
- Intended Use/ User Needs: The subject devices were validated with intended users in cadaver labs or simulated use tests to ensure the user needs and intended use requirements were met. All requirements were met and no new issues of safety or effectiveness were raised.
- Accuracy: The System is designed to work in the working space with a mean accuracy of 2 mm point and 2° angular axis displacement within the registration zone. The 95th percentile of the point displacement is ≤ 3 mm and ≤ 3° for angular axis displacement within the registration zone.
Positional Displacement (mm): Mean 1.32, Standard Deviation 0.52, 99% Confidence Interval (Upper) 2.60
Trajectory Angle Displacement (degrees): Mean 0.73, Standard Deviation 0.43, 99% Confidence Interval (Upper) 1.78 - Safety: Verified the effectiveness of all risk controls determined in the device risk analysis. No new issues of safety or effectiveness were raised.
- General Requirements and Performance: Verified all components against their design specifications. All requirements were met and no new issues of safety or effectiveness were raised.
- Software: Software verification and validation testing was conducted as required by IEC 62304 and FDA guidance on general principles of software validation, January 11, 2002. All requirements were met and no new issues of safety or effectiveness were raised.
- Biocompatibility: The biocompatibility of all patient contact materials was verified according to ISO 10993-1:2018 and FDA guidance on the use of ISO 10993-1, September 2020. No new issues of safety or effectiveness were raised.
- Electrical Safety: Verified conformance to IEC 60601-1: 2005, COR. 1:2006, COR. 2:2007, AMD 1:2012 (equivalent to IEC 60601-1:2012 Reprint).
- Electromagnetic Compatibility: Verified conformance to IEC 60601-1-2: 2014, CISPR 11 Group 1, Class A requirements as well as additional testing to verify compatibility with RFID devices operating in the 125 - 134 kHz and 13.56 MHz frequency band.
- Shipping: The functionality of the devices after simulated shipping conditions was verified. No new issues of safety or effectiveness were raised.
- Sterilization: The reusable subject devices underwent a steam sterilization validation to demonstrate that they can be expected to be sterile and have a sterility assurance level (SAL) of 10-6 or greater after processing. All requirements were met and no new issues of safety or effectiveness were raised.
No clinical testing was performed.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Mean accuracy of 2 mm for positional displacement and 2° for trajectory angle displacement.
The 95th percentile of the point displacement is ≤ 3 mm and ≤ 3° for angular axis displacement within the registration zone.
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 882.4560 Stereotaxic instrument.
(a)
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.(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.
May 27, 2022
Stryker Leibinger GmbH & Co. KG Andrea Wallen-Gerding Principal Regulatory Affairs Specialist Bötzinger Straße 41 Freiburg, Baden-Wurttemberg D-79111 Germany
Re: K220593
Trade/Device Name: Spine Guidance Software, Q Guidance System Regulation Number: 21 CFR 882.4560 Regulation Name: Stereotaxic Instrument Regulatory Class: Class II Product Code: OLO Dated: February 28, 2022 Received: March 1, 2022
Dear Andrea Wallen-Gerding:
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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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.
1
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 of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely.
Shumaya Ali, M.P.H. Assistant Director DHT6C: Division of Restorative, Repair and Trauma Devices OHT6: Office of Orthopedic Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known) K220593
Device Name Spine Guidance Software
Indications for Use (Describe)
The Stryker Q Guidance System, when used with the Spine Guidance software, is intended as a planning and intraoperative guidance system to enable open or percutaneous computer assisted surgery in adult and pediatric (adolescent) patients.
The system is indicated for any surgical procedure on the spine in which the use of computer assisted planning and surgery may be appropriate. The system can be used for intraoperative guidance where a reference to a rigid anatomical structure such as the spine, pelvis or skull can be identified.
The system assists in the positioning of instruments for procedures on the spine and pelvis, including:
- Screw Placement in the spine or pelvis
Type of Use (Select one or both, as applicable)> Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
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DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
3
Indications for Use
510(k) Number (if known) K220593
Device Name
· Guidance System
Indications for Use (Describe)
The Q Guidance System is intended as an aid for precisely locating anatomical structures in open or percutaneous computer assisted surgery. The system is indicated for any medical condition in which the use of computer assisted planning and surgery may be appropriate and where reference to a rigid anatomical structure such as the skull, vertebra, or long bone can be identified.
Type of Use (Select one or both, as applicable)
| Prescription Use (Part 21 CFR 801 Subpart D) |
|---|
| Over-The-Counter Use (21 CFR 801 Subpart C) |
CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
4
Submitter Information 6.0
This Premarket Notification is submitted by: 6.1
Stryker Leibinger GmbH & Co. KG Bötzinger Straße 41 79111 Freiburg, Germany
Contact Information 6.2
| Contact Name: | Andrea N. Wallen-Gerding |
|---|---|
| Cell Telephone: | (269) 491-9234 |
| Email: | andrea.wallengerding@stryker.com |
| Date Prepared: | February 28, 2022 |
Device Name 6.3
Table 6-1: Device Name
| Subject (Modified) Device Information | |
|---|---|
| Trade/ Proprietary Name | Spine Guidance Software |
| Q Guidance System | |
| Common Name | Stereotaxic Instruments |
| Classification | Class II |
| Classification Product Code | OLO |
| Classification Name | Orthopedic Stereotaxic Instrument |
| Classification Regulation | 21 CFR 882.4560 |
| Review Panel | Orthopedic |
Predicate Devices 6.4
The following are the legally marketed predicate devices for the subject device included in this Traditional 510(k):
5
| Subject Device | Predicate Device
Trade Name | 510(k) | Product
Code | Manufacturer |
|--------------------------------|--------------------------------|----------------------|-----------------|------------------------------------|
| Spine Guidance 4.0
Software | SpineMap 3D 3.1
Software | K172034
[Primary] | OLO | Stryker Leibinger
GmbH & Co. KG |
| Stryker Q Guidance
System | Stryker NAV3i
Platform | K162341 | OLO | Stryker Leibinger
GmbH & Co. KG |
Table 6-2: Predicate Device List
Device Description 6.5
Stryker Q Guidance System with Spine Guidance 4.0 Software System 6.5.1 Overview
The Stryker Q Guidance System with Spine Guidance 4.0 Software system is a computer-assisted stereotaxic, image-guided, planning, and intraoperative guidance system intended to enable open or percutaneous computer-assisted surgery. It assists the surgeon in precisely positioning instruments and locating patient anatomy during spinal surgery.
The Q Guidance System with Spine Guidance 4.0 Software system is comprised of a computer platform, Spine Guidance Software, navigated accessories/ instruments (e.g., patient/ instrument trackers, pointers), and various system components (i.e. Calibration Body, Registration Pointer, etc.). The system provides intraoperative guidance to the surgeon using passive and active wireless optical tracking technologies. The computer platform consists of a computer, camera, big touchscreen monitor, and a small touchscreen monitor.
The Spine Guidance 4.0 Software is dedicated to spine surgical procedures as defined in the indications for use. Required navigated instruments include a patient tracker, an instrument tracker, pointers, etc. An instrument battery is required when a battery powered instrument or calibration device is used.
The Spine Guidance 4.0 Software displays the intraoperative location of navigated surgical instruments relative to imported patient medical images via wireless optical tracking technology. The software provides the functions to perform the indicated navigated spine surgical procedures. The software guides the user through the necessary preoperative and intraoperative steps required to set-up and perform the navigated spine surgical procedures.
The Spine Guidance 4.0 Software system includes the system components described below.
- Flat Disc Stick-On Fiducials A
The Flat Disc Stick-On Fiducials are passive imaging device trackers designed specifically for use with the AIRO Mobile TruCT System. The Flat Disc Stick-On Fiducials combine to form a
Traditional 510(k)
6
passive tracker used for automatically registering patient image data with the patient tracker in place.
-
A Calibration Body
The Calibration Body is used to validate and calibrate active and passive optically navigated instruments when used with the Spine Guidance Software system. -
A Registration Pointer
The Registration Pointers are optional accessories to the Spine Guidance Software. They include pins for the connection of reflective spheres that allow them to be tracked by the Spine Guidance Software system. -
A Mayfield Base with Articulating Arm
The Mayfield Base with Articulating Arm has a mechanical interface to the starburst connection on skull clamps. A Universal Tracker or an nGenius Universal Tracker can be attached to the Mayfield Base with Articulating Arm to enable tracking by the Spine Guidance Software system.
6.6 Indications for Use
6.6.1 Stryker Q Guidance System
The O Guidance System is intended as an aid for precisely locating anatomical structures in open or percutaneous computer assisted surgery. The system is indicated for any medical condition in which the use of computer assisted planning and surgery may be appropriate and where reference to a rigid anatomical structure such as the skull, vertebra, or long bone can be identified.
Spine Guidance 4.0 Software 6.6.2
The Stryker O Guidance System, when used with the Spine Guidance software, is intended as a planning and intraoperative guidance system to enable open or percutaneous computer assisted surgery in adult and pediatric (adolescent) patients.
The system is indicated for any surgical procedure on the spine in which the use of computer assisted planning and surgery may be appropriate. The system can be used for intraoperative guidance where a reference to a rigid anatomical structure such as the spine, pelvis or skull can be identified.
The system assists in the positioning of instruments for procedures on the spine and pelvis, including:
- Screw Placement in the spine or pelvis ●
Comparison of Technological Characteristics 6.7
A comparison of the technological characteristics of the subject devices included in the scope of this Traditional 510(k) is included in the tables below.
Traditional 510(k)
7
6.7.1 Technological Comparison between the Stryker Spine Guidance 4.0 Software System and the Stryker SpineMap 3D 3.1 Software System
The technological comparison between the subject device (Stryker Spine Guidance Software System) and the predicate device (SpineMap 3D 3.1 Software System) is included in Table 6-3 below. The Stryker Navigation System with SpineMap 3D 3.1 software application received 510(k) clearance per 510(k) number K172034.
| Table 6-3: Technological Comparison between Stryker Q Guidance System with Spine Guidance 4.0 |
|---|
| Software (Subject Device) and the Predicate Device |
| Item | Subject Device:
Stryker Q Guidance System with Spine
Guidance 4.0 Software | Predicate Device:
Stryker Navigation System with
SpineMap 3D 3.1 Software Application
(K172034) |
|------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Indications
for Use | The Stryker Q Guidance System, when
used with the Spine Guidance Software,
is intended as a planning and
intraoperative guidance system to enable
open or percutaneous computer assisted
surgery in adult and pediatric patients.
The system is indicated for any surgical
procedure on the spine in which the use
of computer assisted planning and surgery
may be appropriate. The system can be
used for intraoperative guidance where a
reference to a rigid anatomical structure
such as the spine, pelvis or skull can be
identified.
The system assists in the positioning of
instruments for procedures on the spine
and pelvis, including:
• Screw Placement in the spine or
pelvis | The Stryker Navigation System, when
used with the SpineMap 3D software
application, is intended as a planning and
intraoperative guidance system to enable
open or percutaneous computer assisted
surgery.
The system is indicated for any medical
condition in which the use of computer
assisted planning and surgery may be
appropriate. The system can be used for
intraoperative guidance where a reference
to a rigid anatomical structure such as the
pelvis or spine can be identified.
The system assists in the positioning of
instruments for procedures on the pelvis
and spine, including:
• Screw Placement in the spine, ilium,
or pelvis |
| Main System
Components | • Q Guidance System
• Spine Guidance 4.0 Software
• Navigated Instruments
• System accessories and components | • NAV3 Platform Family
• SpineMap 3D 3.1 Software
• Navigated Instruments
• System accessories and components |
| Modes of
Operation | • Patient Preparation
• System Set-up
• Image Import
• Planning
• Patient Registration
• Navigation | • Patient Preparation
• System Set-up
• Image Import
• Planning
• Patient Registration
• Navigation |
| Item | Subject Device:
Stryker Q Guidance System with Spine
Guidance 4.0 Software | Predicate Device:
Stryker Navigation System with
SpineMap 3D 3.1 Software Application
(K172034) |
| Localizing
and Tracking
Technology | Infrared Optical Active Tracking:
Infrared light emitted by diodes placed in
specific locations on tracked instruments
is sensed by the navigation camera on the
platform, which allows for computation
of the position and orientation of the
tracked instruments.
Infrared Optical Passive Tracking:
Infrared light from reflective navigation
spheres or discs in specific locations on
tracked instruments or imaging devices
are sensed by the navigation camera on
the platform, which allows for
computation of the position and
orientation of the tracked instruments.
The navigation camera sends out regular
infrared light pulses which are reflected
by the navigation spheres on the tracked
instruments. | Infrared optical active sensing
technology: Infrared light emitted by
diodes placed in specific locations on
navigated surgical instruments is sensed
by a camera array (navigation camera) on
the platform, which allows for
computation of the spatial information |
| Operating
Principle | • The software is installed on the
computer that is part of the platform
• Images are imported in DICOM format
• The software displays the images and
planned items with navigational
information on a monitor | • The software is installed on the
computer that is part of the platform
• Images are imported in DICOM format
• The software displays the images and
planned items with navigational
information on a monitor |
| System
Accuracy | The system has a mean accuracy of 2 mm
for positional displacement and 2° for
trajectory angle displacement. Accuracy
values apply to tracking in the workspace. | The system has a mean accuracy of 2 mm
for positional displacement and 2° for
trajectory angle displacement. Accuracy
values apply to tracking in the workspace. |
| Supported
Imaging
Modalities | • Computed tomography (CT)
• Computed tomography angiography
(CTA)
• Magnetic resonance (MR)
• Magnetic resonance angiography
(MRA)
• Position emission tomography (PET) | • Computed tomography (CT)
• Computed tomography angiography
(CTA)
• Magnetic resonance (MR)
• Magnetic resonance angiography
(MRA)
• Position emission tomography (PET) |
| Planning
Features | • Screws
• Measurement
• Trajectories
• Automatic Segmentation
• Manual Segmentation
• Merge Levels (Local Correlation)
• Image Merge | • Screws
• Measurements
• Planes
• Annotation Points
• Trajectories
• Manual Segmentation
• Anatomical Systems
• Local Correlation
• Image Merge |
| Item | Subject Device:
Stryker Q Guidance System with Spine
Guidance 4.0 Software | Predicate Device:
Stryker Navigation System with
SpineMap 3D 3.1 Software Application
(K172034) |
| Registration
Features | · Anatomical (Point-to-Point)
Registration
· Surface Registration
· 3D CT/C-Arm Registration
· Automatic Intraoperative Mask
Registration which includes AIM
Fallback Workflow
· Mask Registration | · 3D Models
· Compositions
· Anatomical (Point-to-Point)
Registration
· Surface Registration
· 3D C-Arm Registration
· Automatic Intraoperative Mask (AIM)
Registration which includes the AIM
Fallback Workflow
· Mask Registration |
| Energy
Source | · Main Power: Alternating Current (AC)
power supply, 100/240 V and 50/60 Hz
· Uninterruptable Power supply with
battery support for 6 minutes | · Main Power: Alternating Current (AC)
power supply, 100/240 V and 50/60 Hz
· Off-the-Shelf uninterruptable power
supply for power interruptions ≤ 6
minutes |
| Intended Use
Environment | Operating Room (OR) | Operating Room (OR) |
| Input | · Analog Video Input (AVI)
· Digital Video Input (DVI)
· Ethernet
· USB | · Analog Video Input (AVI)
· Ethernet
· USB |
| Output | · 3D image
· Analog and Digital Video Images (e.g.,
endoscopy, target guidance image) | · 3D image,
· Anatomic orthogonal images,
· Analog video image (e.g., endoscopy,
target guidance image) |
| Graphical
User
Interface | · Black-style graphical user interface
· 16:9 screen ratio
· Case Dashboard to access all operation
modes
· Image box with image tools
· Current task panel on the right
· Image settings task panel on the left | · Black-style graphical user interface
· 16:9 screen ratio
· One tab per task concept from left to
right on top of screen
· Image box with image tools
· Current task panel on the right |
| User
Interface | · Large touch monitor
· Small touch monitor
· Keyboard
· Mouse
· Buttons on active optical instruments | · Monitor with resolution display screen
· Virtual keyboard
· Mouse
· IO Tablet with touch screen, USB
ports, and CD/DVD drive
· Buttons on Navigated Instruments |
8
9
10
Summary of Non-Clinical Testing 6.8
The function and performance of the subject devices (i.e., Stryker Q Guidance System with Spine Guidance Software (including the system components listed above) have been evaluated through non-clinical design verification and validation testing. The results of the evaluation tests demonstrate that the subject devices successfully meet the requirements of their intended use.
Additional testing was performed on the subject devices to ensure they met their design requirements. A summary of the testing and the results are included in the table below.
| Item | Summary of Testing | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Intended Use/ User Needs | The subject devices were validated with intended users in cadaver labs or simulated use tests to ensure the user needs and intended use requirements were met. All requirements were met and no new issues of safety or effectiveness were raised. | ||||||||||||
| Accuracy | The System is designed to work in the working space with a mean accuracy of 2 mm point and 2º angular axis displacement within the registration zone. The 95th percentile of the point displacement is ≤ 3 mm and ≤ 3° for angular axis displacement within the registration zone. | ||||||||||||
| Positional | |||||||||||||
| Displacement (mm) Trajectory Angle | |||||||||||||
| Displacement (degrees) 99% Confidence | |||||||||||||
| Interval (Upper) 2.60 1.78 Mean 1.32 0.73 Standard Deviation 0.52 0.43 | |||||||||||||
| Safety | Verified the effectiveness of all risk controls determined in the device risk analysis. No new issues of safety or effectiveness were raised. | ||||||||||||
| General Requirements and | |||||||||||||
| Performance | Verified all components against their design specifications. All requirements were met and no new issues of safety or effectiveness were raised. | ||||||||||||
| Software | Software verification and validation testing was conducted as required by IEC 62304 and FDA guidance on general principles of software validation, January 11, 2002. All requirements were met and no new issues of safety or effectiveness were raised. | ||||||||||||
| Biocompatibility | The biocompatibility of all patient contact materials was verified according to ISO 10993-1:2018 and FDA guidance on the use of ISO 10993-1, September 2020. No new issues of safety or effectiveness were raised. | ||||||||||||
| Electrical Safety | Verified conformance to IEC 60601-1: 2005, COR. 1:2006, COR. 2:2007, AMD 1:2012 (equivalent to IEC 60601-1:2012 Reprint). | ||||||||||||
| Electromagnetic Compatibility | Verified conformance to IEC 60601-1-2: 2014, CISPR 11 Group 1, Class A requirements as well as additional testing to verify |
11
| Item | Summary of Testing |
|---|---|
| compatibility with RFID devices operating in the 125 - 134 kHz and | |
| 13.56 MHz frequency band. | |
| Shipping | The functionality of the devices after simulated shipping conditions |
| was verified. No new issues of safety or effectiveness were raised. | |
| Sterilization | The reusable subject devices underwent a steam sterilization |
| validation to demonstrate that they can be expected to be sterile and | |
| have a sterility assurance level (SAL) of 10-6 or greater after | |
| processing. All requirements were met and no new issues of safety or | |
| effectiveness were raised. |
Summary of Clinical Testing 6.9
No clinical testing was performed.
6.10 Conclusion
The subject devices, Stryker Q Guidance System and Spine Guidance 4.0 Software, including the system components described above, perform as intended and are substantially equivalent to their respective predicate device with regard to intended use, design, principles of operation, technology, materials, and performance. No new issues of safety or effectiveness have been raised.