Browse hierarchy: [Orthopedic (OR)](/submissions/OR) → [Subpart B — Diagnostic Devices](/submissions/OR/subpart-b%E2%80%94diagnostic-devices) → [21 CFR 888.1150](/submissions/OR/subpart-b%E2%80%94diagnostic-devices/888.1150) → SIT — Arthroscopic Or Orthopedic Endoscopic Intraoperative Augmented Reality Video See-Through Display System

# SIT · Arthroscopic Or Orthopedic Endoscopic Intraoperative Augmented Reality Video See-Through Display System

_Orthopedic · 21 CFR 888.1150 · Class 2_

**Canonical URL:** https://fda.innolitics.com/productcode/SIT

## Overview

- **Product Code:** SIT
- **Device Name:** Arthroscopic Or Orthopedic Endoscopic Intraoperative Augmented Reality Video See-Through Display System
- **Regulation:** [21 CFR 888.1150](/submissions/OR/subpart-b%E2%80%94diagnostic-devices/888.1150)
- **Device Class:** 2
- **Review Panel:** [Orthopedic](/submissions/OR)

## Identification

SportSuite Vision Software is an arthroscopic or orthopedic endoscopic intraoperative augmented reality video see-through display system. It consists of augmented reality software on a head-mounted display that displays arthroscopic or endoscopic video and medical imaging during orthopedic surgery, specifically for femoroacetabular impingement and labral repair hip arthroscopy procedures. The device is intended to intraoperatively augment visualization with contextually relevant information and data, including that received from other devices.

## Classification Rationale

FDA concludes that this device should be classified into Class II. This order classifies the device into Class II with the establishment of special controls, which provide reasonable assurance of the safety and effectiveness of the device type.

## Recent Cleared Devices (1 of 1)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [DEN250040](/device/DEN250040.md) | SportSuite Vision Software | Stryker Endoscopy | Jul 17, 2026 | DENG |

## Top Applicants

- Stryker Endoscopy — 1 clearance

---

**Source:** [https://fda.innolitics.com/productcode/SIT](https://fda.innolitics.com/productcode/SIT)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com
