Search Results

Ask a specific question about this device

Ask a specific question about this device

IRISeg is intended for use as a software application that receives DICOM compliant MR or contrast-enhanced CT images, provides manual and machine learning-enabled tools for image analysis and segmentation, and creates an output file that can be used to render a 3D model for preoperative surgical planning and intraoperative display. The use of IRISeg may include the generation of preliminary segmentations using machine learning algorithms. IRISeg is intended for use by qualified professionals. The output file is meant for visual, non-diagnostic use and shall be reviewed by clinicians who are responsible for all final patient management decisions.

The machine learning enabled kidney CT auto-segmentation tool is intended for use for adult patients with contrast-enhanced, axial kidney CT images with slice thickness 3mm or less.

IRISeg is a standalone software application created by Intuitive Surgical for segmentation of CT and MR images and generation of output files that can be rendered as virtual 3D models of anatomical structures. IRISeg is designed to provide qualified professionals ("users") with a machine learning (ML)-based tool for auto-segmentation of kidney anatomy based on CT scans and non-ML manual tools for segmentation based on CT and MR scans.

Note that there have been no changes to existing tools or introductions of new tools between the predicate and subject devices.

Input File
IRISeg can open and load CT or MR imaging files in DICOM (Digital Imaging and Communications in Medicine) format, and segmentation label files in NIfTI (Neuroimaging Informatics Technology Initiative) format from an accessible storage location.

Output File
Following the use of IRISeg to segment CT or MR imaging files, the software can be used to generate an output file that can be used to render virtual segmented 3D models.

IRISeg Manual Tools
IRISeg includes a variety of tools for users to manually edit segmentation labels, such as Paintbrush tools, Eraser tools, Connected Component Selection, Free Curve Selection, Morphological operations, Mathematical Operations.

Manual tools alone can be used to manually segment (annotate) CT and MR scans.

Manual tools can also be used to modify the output of the ML-based auto-segmentation algorithm. The ML-based auto-segmentation does not generate mass labels. Users must segment and label renal masses using manual tools.

IRISeg ML-Based Auto-Segmentation Tool
IRISeg includes an ML-based auto-segmentation algorithm (cleared under K242461 and unchanged in the subject device) for automatic segmentation of four kidney structures from CT imaging. The auto-segmentation algorithm is a neural network based ML algorithm. It is trained on segmented kidney CT models that were sourced from clinical data processed during commercial operation of the cleared IRIS 1.0 system (K182643). Each 3D model was reviewed by one U.S board certified radiologist. The input is a CT image (series of 2D slices). The output of the model is four probability maps for kidney parenchyma, kidney artery, kidney vein, and collecting system. The probability maps are thresholded to generate binary masks for kidney parenchyma, kidney artery, kidney vein and collecting system. The ML-based auto-segmentation does not generate binary masks for kidney masses.

The algorithm output is intended as an initial estimate of the segmentation. The user must use the manual tools to update the initial algorithm output to generate the kidney CT 3D model.

The development of the IRISeg kidney CT ML-based auto-segmentation algorithm followed FDA's Good Machine Learning Practices for Medical Device Development: Guiding Principles, October 2021.

This 510(k) clearance letter pertains to IRISeg, a software application that assists in the segmentation of CT and MR images to create 3D models for surgical planning. The document heavily references a predicate device (K242461) as the software itself (including the ML-based auto-segmentation algorithm) has not changed. The clearance addresses the expansion of the indications for use to include MR images for manual segmentation and the standalone nature of the software.

Here's a breakdown of the requested information based on the provided text:

1. Table of Acceptance Criteria and Reported Device Performance

The provided document doesn't explicitly state quantitative acceptance criteria for the subject device (K251763) beyond "all tests met the acceptance criteria" in reference to general software testing. However, it does state that the ML auto-segmentation algorithm was "not modified in the subject device, and therefore the performance of the ML algorithm is as effective as in the predicate device."

To address the request, we would need to infer information from the predicate device's clearance (K242461), which is not fully detailed in this document. Since the ML algorithm remains the same, any performance metrics from K242461 would be applicable. However, without details from K242461, we can only report what is explicitly mentioned here about K251763.

The document notes that the "ML-based auto-segmentation does not generate mass labels" and "Users must segment and label renal masses using manual tools." This is a limitation, not a performance metric, but relevant to the overall utility.

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

For ML Auto-Segmentation (performance inherited from K242461):

• Test Set Sample Size: Not explicitly stated for K251763 or K242461. The document only mentions the training data for the ML model.
• Data Provenance: Not explicitly stated for the test set.

For Manual Segmentation and General Software Testing (K251763):

• Test Set Sample Size: Not explicitly stated.
• Data Provenance: Not explicitly stated.

The document indicates that the machine learning model was trained on "clinical data processed during commercial operation of the cleared IRIS 1.0 system (K182643)." This suggests real-world clinical data, likely retrospective. The country of origin is not specified but given "U.S. board certified radiologist," it's reasonable to infer the data includes U.S. clinical data.

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

For ML Auto-Segmentation (training data from IRIS 1.0, K182643):

• Number of Experts: "one U.S board certified radiologist" per 3D model.
• Qualifications: U.S. board certified radiologist. Years of experience are not specified.

For the test set(s) used for K251763 (functional, usability, cybersecurity, and manual segmentation for MR):

• Number of Experts/Users for Ground Truth: Not explicitly stated. The document refers to "qualified professionals" as intended users, who would perform manual segmentation tasks.

4. Adjudication Method for the Test Set

For ML Auto-Segmentation (training data ground truth from IRIS 1.0, K182643):

• Adjudication Method: "Each 3D model was reviewed by one U.S board certified radiologist." This implies a single-reader ground truth without explicit adjudication unless that review process involved an internal review cycle. No 2+1 or 3+1 method is mentioned.

For the test set(s) used for K251763:

• Adjudication Method: Not explicitly stated for any of the general software testing.

5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study

• Was an MRMC study done? No, an MRMC comparative effectiveness study is not mentioned or described in the provided text.
• Effect size of improvement: Not applicable, as no MRMC study was conducted or reported. The document focuses on the standalone algorithm's performance and the general software functionality.

6. Standalone (Algorithm Only Without Human-in-the-Loop) Performance

• Was standalone performance done? Yes, implicitly. The document states: "The output of the model is four probability maps for kidney parenchyma, kidney artery, kidney vein, and collecting system. The probability maps are thresholded to generate binary masks..." This describes the direct output of the ML algorithm.
  • It also clarifies: "The algorithm output is intended as an initial estimate of the segmentation. The user must use the manual tools to update the initial algorithm output to generate the kidney CT 3D model." This indicates that while standalone output exists, it is expected to be refined by a human.
  • Performance for "Machine Learning Auto-Segmentation Testing" is specifically mentioned under K242461, and stated to be the "Same" for K251763. However, specific performance metrics (e.g., Dice coefficient, sensitivity, specificity) for this standalone performance are not provided in this document.

7. Type of Ground Truth Used

For ML Auto-Segmentation Training Set:

• Type of Ground Truth: Expert consensus (specifically, review by "one U.S board certified radiologist" per model). This is a form of expert annotation/segmentation.

For the test set(s) of K251763:

• Type of Ground Truth: Not explicitly stated for the general software testing. For manual segmentation, it would likely involve expert-derived reference segmentations or user-defined targets.

8. Sample Size for the Training Set

• Sample Size for Training Set: Not explicitly stated. The document mentions training on "segmented kidney CT models that were sourced from clinical data processed during commercial operation of the cleared IRIS 1.0 system (K182643)," but the number of such models is not provided.

9. How the Ground Truth for the Training Set Was Established

• How Ground Truth Was Established: "Each 3D model [used for training the ML-algorithm] was reviewed by one U.S board certified radiologist." This indicates that a U.S. board-certified radiologist manually segmented or reviewed and confirmed the segmentation of the 3D models used as ground truth for training.

Ask a specific question about this device

The Intuitive Surgical Endoscopic Instrument Control System (da Vinci SP Surgical System, Model SP1098) is intended to assist in the accurate control of Intuitive Surgical da Vinci SP Instruments during urologic, colorectal, and general thoracoscopic surgical procedures that are appropriate for a single port approach; and transoral otolaryngology surgical procedures in the oropharynx restricted to benign tumors and malignant tumors classified as T1 and T2. The system is also indicated for use in nipple sparing mastectomy (NSM) procedures. The system is indicated for adult use. It is intended for use by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

Intuitive Surgical da Vinci SP Instruments are controlled by the da Vinci SP Surgical System, Model SP1098, and include flexible endoscopes, blunt and sharp endoscopic dissectors, scissors, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, and suturing through a single port. The system is indicated for urologic, colorectal, and general thoracoscopic surgical procedures that are appropriate for a single port approach; and transoral otolaryngology surgical procedures in the oropharynx restricted to benign tumors and malignant tumors classified as T1 and T2. The system is also indicated for use in nipple sparing mastectomy (NSM) procedures. The system is indicated for adult use. It is intended for use by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

The da Vinci SP Surgical System is designed to enable complex surgical procedures using a minimally invasive approach. The system consists of a Surgeon Console, a Vision Cart, and a Patient Cart and is used with an endoscope, instruments, and accessories.

The surgeon seated at the Surgeon Console controls all movement of the instruments and endoscope by using two hand controls and a set of foot pedals. The surgeon views the endoscopic image on a three-dimensional (3D) viewer, which provides a view of patient anatomy and instrumentation, along with icons and other user interface features.

The Vision Cart includes supporting electronic equipment, such as the light source, video and image processing, and the networking hardware. The Vision Cart also has a touchscreen to view the endoscopic image and adjust system settings.

The Patient Cart is the operative component of the da Vinci SP Surgical System. Its primary function is to support the positioning of the surgical port and to manipulate the surgical instruments and endoscope. The Patient Cart is positioned beside the operating room table and contains an instrument arm that is positioned with respect to the target patient anatomy. The instrument arm contains four instrument drives that hold up to three surgical instruments and the endoscope. The bedside surgical assistant installs and removes the endoscope and instruments intra-operatively as needed.

This 510(k) is for a labeling modification only, to add "nipple sparing mastectomy (NSM) procedures" to the indications, and to add "nipple sparing mastectomy" as new representative, specific procedures in the Professional Instructions for Use. There have been no technical changes to the device.

N/A

Ask a specific question about this device

da Vinci SP Surgical System, Model SP1098:

The Intuitive Surgical Endoscopic Instrument Control System (da Vinci SP Surgical System, Model SP1098) is intended to assist in the accurate control of Intuitive Surgical da Vinci SP Instruments during urologic, colorectal, and general thoracoscopic surgical procedures that are appropriate for a single port approach; and transoral otolaryngology surgical procedures in the oropharynx restricted to benign tumors and malignant tumors classified as T1 and T2. The system is also indicated for use in cholecystectomy, inguinal hernia repair, and appendectomy procedures. The system is indicated for adult use. It is intended for use by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

da Vinci SP Instruments:

Intuitive Surgical da Vinci SP Instruments are controlled by the da Vinci SP Surgical System, Model SP1098, and include flexible endoscopes, blunt and sharp endoscopic dissectors, scissors, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, and suturing through a single port. The system is indicated for urologic, colorectal, and general thoracoscopic, surgical procedures that are appropriate for a single port approach; and transoral otolaryngology surgical procedures in the oropharynx restricted to benign tumors and malignant tumors classified as T1 and T2. The system is also indicated for use in cholecystectomy, inguinal hernia repair, and appendectomy procedures. The system is indicated for adult use. It is intended for use by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

The da Vinci SP Surgical System is designed to enable complex surgery using a minimally invasive approach. The system consists of a Surgeon Console, a Vision Cart, and a Patient Cart and is used with an endoscope, instruments, and accessories.

The surgeon seated at the Surgeon Console controls all movement of the instruments and endoscope by using two hand controls and a set of foot pedals. The surgeon views the endoscopic image on a three-dimensional (3D) viewer, which provides a view of patient anatomy and instrumentation, along with icons and other user interface features.

The Vision Cart includes supporting electronic equipment, such as the light source, video and image processing, and the networking hardware. The Vision Cart also has a touchscreen to view the endoscopic image and adjust system settings.

The Patient Cart is the operative component of the da Vinci SP Surgical System. Its primary function is to support the positioning of the surgical port and to manipulate the surgical instruments and endoscope. The Patient Cart is positioned at the operating room and contains an instrument arm that is positioned with respect to the target patient anatomy. The instrument arm contains four instrument drives that hold up to three surgical instruments and the endoscope. The patient-side assistant installs and removes the endoscope and instruments intra-operatively.

This 510(k) is for a labeling modification only, to add "cholecystectomy, inguinal hernia repair, and appendectomy" to the cleared labeling.

N/A

Ask a specific question about this device

da Vinci SP Surgical System, Model SP1098:
The Intuitive Surgical Endoscopic Instrument Control System (da Vinci SP Surgical System, Model SP1098) is intended to assist in the accurate control of Intuitive Surgical EndoWrist SP Instruments during urologic, colorectal, and general thoracoscopic surgical procedures that are appropriate for a single port approach; and transoral otolaryngology surgical procedures in the oropharynx restricted to benign tumors and malignant tumors classified as T1 and T2. The system is indicated for adult use. It is intended for use by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

EndoWrist SP Instruments:
Intuitive Surgical EndoWrist SP Instruments are controlled by the da Vinci SP Surgical System, Model SP1098, and include flexible endoscopes, blunt and sharp endoscopic dissectors, scissors, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, and suturing through a single port. The system is indicated for urologic, colorectal, and general thoracoscopic surgical procedures that are appropriate for a single port approach; and transoral otolaryngology surgical procedures in the oropharynx restricted to benign tumors and malignant tumors classified as T1 and T2. The system is indicated for adult use. It is intended for use by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

The da Vinci SP Surgical System is a robotically-assisted surgical device that is designed to enable complex surgery using a minimally-invasive approach. The system consists of three major subsystems: a Surgeon Console, a Vision Cart, and a Patient Cart.

At the Surgeon Console, the surgeon controls all movement of the instruments and endoscope by using two hand controls and a set of foot pedals. The surgeon views the live endoscope image on a three-dimensional (3D) viewer, which provides a view of patient anatomy and instrumentation, along with icons and other user interface features.

The Vision Cart includes supporting electronic equipment, such as the endoscope light source, video and image processing, and the networking hardware. The Vision Cart also has a touchscreen to view the endoscope image and adjust system settings.

The Patient Cart is the operative component of the da Vinci SP Surgical System. It supports the positioning of the surgical port and manipulation of the surgical instruments and endoscope.

N/A

Ask a specific question about this device

The Ion™ Endoluminal System (Model IF1000) assists the user in navigating a catheter and endoscopic tools in the pulmonary tract using endoscopic visualization of the tracheobronchial tree for diagnostic and therapeutic procedures. The Ion™ Endoluminal System enables fiducial marker placement. It does not make a diagnosis and is not for pediatric use.

The PlanPoint™ Software uses patient CT scans to create a 3D plan of the lung and navigation pathways for use with the Ion™ Endoluminal System.

The Ion Endoluminal System, Model IF1000, is a software-controlled, electro-mechanical system designed to assist qualified physicians to navigate a catheter and endoscopic tools in the pulmonary tract using endoscopic visualization of the tracheobronchial tree for diagnostic and therapeutic procedures. It consists of a Planning Laptop with PlanPoint Software, a System Cart with System Software, a Controller, Instruments, and Accessories.

The IF1000 Instruments include the Ion Fully Articulating Catheter, the Ion™ Peripheral Vision Probe, and the Flexision Biopsy Needles.

The Planning Laptop is a separate computer from the System Cart and Controller. A 3D airway model is generated from the patient's chest CT scan using the PlanPoint Software.

The System Cart contains the Instrument Arm, electronics for the follower portion of the servomechanism, and two monitors. The System Cart allows the user to navigate the Catheter Instrument with the Controller, which represents the leader in the leader-follower relationship. For optimal viewing, the physician can position the monitors in both vertical and horizontal axes.

The Controller is the user input device on the Ion Endoluminal System. It provides the controls to command insertion, retraction, and articulation of the Catheter. The Controller also has buttons to operate the Catheter control states.

The Ion Endoluminal System integrates an optional Tomosynthesis feature, optimizes the existing Cone Beam CT workflow, improves the Navigation View, troubleshoots the airway tree, and enhances the control algorithm to provide an additional safety margin.

N/A

Ask a specific question about this device

da Vinci SP Surgical System, Model SP1098

The Intuitive Surgical Endoscopic Instrument Control System (da Vinci SP Surgical System, Model SP1098) is intended to assist in the accurate control of Intuitive Surgical EndoWrist SP Instruments during urologic, colorectal, and general thoracoscopic surgical procedures that are appropriate for a single port approach, and transoral otolaryngology surgical procedures in the oropharynx restricted to benign tumors and malignant tumors classified as T1 and T2. The system is indicated for adult use. It is intended for use by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

da Vinci SP Instruments

Intuitive Surgical da Vinci SP Instruments are controlled by the da Vinci SP Surgical System, Model SP1098, and include flexible endoscopes, blunt and sharp endoscopic dissectors, scissors, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, and suturing through a single port. The system is indicated for urologic, colorectal, and general thoracoscopic surgical procedures that are appropriate for a single port approach, and transoral otolaryngology surgical procedures in the oropharynx restricted to benign tumors and malignant tumors classified as T1 and T2. The system is indicated for adult use. It is intended for use by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

The da Vinci SP Surgical System is a robotically-assisted surgical device that is designed to enable complex surgery using a minimally-invasive approach. The system consists of three major subsystems: a Surgeon Console, a Vision Cart, and a Patient Cart.

At the Surgeon Console, the surgeon controls all movement of the instruments and endoscope by using two hand controls and a set of foot pedals. The surgeon views the live endoscope image on a three-dimensional (3D) viewer, which provides a view of patient anatomy and instrumentation, along with icons and other user interface features.

The Vision Cart includes supporting electronic equipment, such as the endoscope light source, video and image processing, and the networking hardware. The Vision Cart also has a touchscreen to view the endoscope image and adjust system settings.

The Patient Cart is the operative component of the da Vinci SP Surgical System. It supports the positioning of the surgical port and manipulation of the surgical instruments and endoscope.

N/A

Ask a specific question about this device

The Intuitive Surgical Endoscopic Instrument Control System (da Vinci Surgical System, Model IS5000) shall assist in the accurate control of Intuitive Surgical Endoscopic Instruments including rigid endoscopes, blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories, during urologic surgical procedures, general laparoscopic surgical procedures, gynecologic laparoscopic surgical procedures and general thoracoscopic surgical procedures. The system is indicated for adult use.

It is intended to be used by trained physicians in an operating room environment in accordance with the representative, specific procedures set forth in the Professional Instructions for Use.

Contraindication:
Use of the force feedback needle driver is contraindicated in hysterectomy and myomectomy due to the risk of vaginal bleeding requiring hospital readmission and/or the need for additional procedures. The use of non-force feedback needle drivers is recommended for suturing in these procedures.

The da Vinci Surgical System, Model IS5000, is a software-controlled, electro-mechanical system designed to enable complex surgery using a minimally invasive approach. The system consists of a Console (Surgeon Console or SSC), a Robot (Patient Side Cart orPSC), and a Tower (Vision Side Cart or VSC) and is used with an endoscope, instruments, and accessories.

The basis for this submission is the initial submission of the da Vinci Surgical System, Model IS5000, cleared under K232610. The device software is being modified to include compatibility support of Harmonic ACE™ Curved Shears. Harmonic ACE™ Curved Shears was previously cleared to be used with da Vinci Surgical Systems Model IS4000 under K143132. This modification does not change the Harmonic ACE™ Curved Shears. It changed the da Vinci Surgical System Model IS5000 software to allow Harmonic ACE™ Curved Shears to be used with the IS5000 system. This modification also includes changes to the da Vinci Surgical System, Model IS5000 device labeling for instruments and accessories.

N/A

Ask a specific question about this device

The Ion™ Endoluminal System (Model IF1000) assists the user in navigating a catheter and endoscopic tools in the pulmonary tract using endoscopic visualization of the tracheobronchial tree for diagnostic and therapeutic procedures. The Ion™ Endoluminal System enables fiducial marker placement. It does not make a diagnosis. The system is indicated for use with adult and pediatric populations. Pediatric use is limited to patients who are 5 ft (152.5 cm) or taller and weigh 102 lbs (46 kg) or greater.

The PlanPoint™ Software uses patient CT scans to create a 3D plan of the lung and navigation pathways for use with the Ion™ Endoluminal System.

The Ion™ Endoluminal System, Model IF1000, is a software-controlled, electromechanical system designed to assist qualified physicians to navigate a catheter and endoscopic tools in the pulmonary tract using endoscopic visualization of the tracheobronchial tree for diagnostic and therapeutic procedures. It consists of a Planning Laptop with PlanPoint™ Software, a System Cart with System Software, a Controller, Instruments, and Accessories. The IF1000 Instruments include the Ion™ Fully Articulating Catheter, the Ion™ Peripheral Vision Probe, and the Flexision™ Biopsy Needles.

The Planning Laptop is a separate computer from the System Cart and Controller. A 3D airway model is generated from the patient's chest CT scan using the PlanPoint™ Software.

The System Cart contains the Instrument Arm, electronics for the follower portion of the servomechanism, and two monitors. The System Cart allows the user to navigate the Catheter Instrument with the Controller, which represents the leader in the leader-follower relationship. For optimal viewing, the physician can position the monitors in both vertical and horizontal axes.

The Controller is the user input device on the Ion™ Endoluminal System. It provides the controls to command insertion, retraction, and articulation of the Catheter. The Controller also has buttons to operate the Catheter control states.

The IF1000 System and PlanPoint Software are modified to enable Remote Software Updates from the Intuitive server via secure network communication.

N/A

Ask a specific question about this device