Dekompressor Percutaneous Discectomy Probe
FDA 510(k) K032473 · Stryker Instruments
510(k) numberK032473
Submission
- Device name
- Dekompressor Percutaneous Discectomy Probe
- Applicant
- Stryker Instruments
Kalamazoo, MI, US - Received
- August 12, 2003
- Decision date
- November 7, 2003
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 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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| K252020 | TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade AssemblyHRX · Traditional | Hand Biomechanics Lab, Inc. | 10/15/2025SE |
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Questions and answers
When was Dekompressor Percutaneous Discectomy Probe cleared by the FDA?
Dekompressor Percutaneous Discectomy Probe (K032473) received a 510(k) decision of Substantially Equivalent on November 7, 2003, 87 days after the submission was received.
What is the product code of K032473?
The FDA product code is HRX – Arthroscope, a Class II (moderate risk) device regulated under 21 CFR 888.1100.