Microchoice Drills and Saws, Micropower Drills and Saws, Micropower Oralmax High Speed Drill
FDA 510(k) K072706 · Conmed Linvatec
510(k) numberK072706
Submission
- Device name
- Microchoice Drills and Saws, Micropower Drills and Saws, Micropower Oralmax High Speed Drill
- Applicant
- Conmed Linvatec
Largo, FL, US - Received
- September 24, 2007
- Decision date
- October 24, 2007
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary 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).
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|---|---|---|---|
| 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.
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| K102339 | Conmed Linvatec Sequent Meniscal Repair DeviceGAT · Traditional | 11/23/2010SE |
| K101100 | Crossft Oc Suture Anchor Mode CFC-4502, CFC-5502, CFC-6502, CFC-4503, CFC-5503, CFC-6503MAI · Traditional | 08/26/2010SE |
| K092898 | Conmed Linvatec Presto Preloaded with One or Two #2 Hi-Fi SuturesMAI · Special | 10/19/2009SE |
| K090560 | Conmed Linvatec Anodized Aluminum Sterilization TraysKCT · Abbreviated | 06/29/2009SE |
| K083161 | Zen Wireless Footswitch (W1000), Zen Wireless Footswitch Adapter (W1100)HRX · Traditional | 03/27/2009SE |
| K080531 | Conmed Linvatec Microfracture Instrument Sterilization TrayKCT · Traditional | 09/05/2008SE |
| K072291 | Conmed Linvatec Bio Mini-Revo Suture AnchorHWC · Traditional | 07/14/2008SE |
| K080444 | Conmed Linvatec Osprey Drill SystemHBC · Traditional | 04/02/2008SE |
Questions and answers
When was Microchoice Drills and Saws, Micropower Drills and Saws, Micropower Oralmax High Speed Drill cleared by the FDA?
Microchoice Drills and Saws, Micropower Drills and Saws, Micropower Oralmax High Speed Drill (K072706) received a 510(k) decision of Substantially Equivalent on October 24, 2007, 30 days after the submission was received.
What is the product code of K072706?
The FDA product code is HRX – Arthroscope, a Class II (moderate risk) device regulated under 21 CFR 888.1100.