Disposable Biopsy Forcep
FDA 510(k) K952630 · Neuro Navigational Corp.
510(k) numberK952630
Submission
- Device name
- Disposable Biopsy Forcep
- Applicant
- Neuro Navigational Corp.
Costa Mesa, CA, US - Received
- June 8, 1995
- Decision date
- September 8, 1995
- 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 |
|---|---|---|
| K965078 | 2.1MM Semi-Rigid Neuroview SCISSORS/2.0OMM Semi-Rigid Neuroview Grasping ForcepsGWG · Traditional | 03/06/1997SE |
| K961406 | Neuroview ScissorsGWG · Traditional | 06/13/1996SE |
| K961300 | Aspiration/Irrigation CatheterGWG · Traditional | 06/07/1996SE |
| K961173 | 1.2MM Reusable Neuroview EndoscopeGWG · Traditional | 06/07/1996SE |
| K960792 | Disposable Neuroview Introducer SheathGWG · Traditional | 04/11/1996SE |
| K954938 | Disposable Neuroview Operating SheathGWG · Traditional | 03/07/1996SE |
| K955351 | Neuroview Coaxial Bipolar ElectrodeGWG · Traditional | 02/29/1996SE |
| K954899 | Rigid Neuroview EndoscopeGWG · Traditional | 12/19/1995SE |
| K955467 | Neuroview Coaxial Bipolar ElectrodeGEI · Traditional | 12/18/1995SE |
| K955037 | Rigid Neuroview EndoscopeHRX · Traditional | 12/04/1995SN |
Questions and answers
When was Disposable Biopsy Forcep cleared by the FDA?
Disposable Biopsy Forcep (K952630) received a 510(k) decision of Substantially Equivalent on September 8, 1995, 92 days after the submission was received.
What is the product code of K952630?
The FDA product code is HRX – Arthroscope, a Class II (moderate risk) device regulated under 21 CFR 888.1100.