Optus Arthroscope & Mini-Arthroscope Accessories
FDA 510(k) K953913 · Optus, Inc.
510(k) numberK953913
Submission
- Device name
- Optus Arthroscope & Mini-Arthroscope Accessories
- Applicant
- Optus, Inc.
Denver, CO, US - Received
- August 21, 1995
- Decision date
- January 22, 1996
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- HRX – Arthroscope
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.1100
- Specialty
- Orthopedic
Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
Other 510(k)s with product code HRX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260203 | Fule Vertebroplasty Balloon CatheterHRX · Traditional | Beijing Fule Science & Technology Development… | 08/28/2026SE |
| K254103 | HOPKINS Telescopes for ArthroscopyHRX · Traditional | Karl Storz SE & CO. KG | 08/26/2026SE |
| K252790 | Digital ClarusScope System and Digital NeuroPEN SystemHRX · Traditional | Clarus Medical, LLC | 05/26/2026SE |
| K253523 | Freedom DS Decompression SystemHRX · Traditional | Spinal Simplicity | 04/16/2026SE |
| K252546 | VantageTM Lumbar Decompression KitHRX · Traditional | Allevion Medical, LLC | 03/12/2026SE |
| K253217 | MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500)…HRX · Traditional | Medimaging Integrated Solution, Inc (Miis) | 12/23/2025SE |
| K250795 | Purevue FMSHRX · Traditional | W.O.M. World of Medicine GmbH | 12/05/2025SE |
| K252666 | Articulator Arthroscopic BurHRX · Traditional | Joint Preservation Innovations, LLC | 11/21/2025SE |
| K252458 | Kyphoplasty Balloon Dilatation CathetersHRX · Traditional | Shanghai Lange Medtech Co., Ltd. | 11/03/2025SE |
| K252020 | TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade AssemblyHRX · Traditional | Hand Biomechanics Lab, Inc. | 10/15/2025SE |
More from Hand Biomechanics Lab, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K945264 | Optus OtoscopesERA · Traditional | 02/02/1996SE |
| K945268 | Optus BronchoscopesEOQ · Traditional | 12/21/1995SE |
| K945265 | Optus Hysteroscopes and Contact HysteroscopesHIH · Traditional | 09/12/1995SE |
| K945262 | Optus Cystoscopes and Pediatric CystoscopesFAJ · Traditional | 05/26/1995SE |
| K945267 | Optus Arthroscopes and Mini-ArthroscopesHRX · Traditional | 05/23/1995SE |
| K945266 | Optus Laparoscopes and Operating LaparoscopesGCJ · Traditional | 02/23/1995SE |
| K944656 | Optus Sinuscopes and AccessoriesEOB · Traditional | 01/26/1995SE |
| K945263 | Optus ThoracoscopesGCJ · Traditional | 12/13/1994SE |
| K945269 | Optus LaryngoscopesCCW · Traditional | 11/07/1994SE |
Questions and answers
When was Optus Arthroscope & Mini-Arthroscope Accessories cleared by the FDA?
Optus Arthroscope & Mini-Arthroscope Accessories (K953913) received a 510(k) decision of Substantially Equivalent on January 22, 1996, 154 days after the submission was received.
What is the product code of K953913?
The FDA product code is HRX – Arthroscope, a Class II (moderate risk) device regulated under 21 CFR 888.1100.