FDA 510(k)

DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE

K-Number: K032473 · 2003-11-07

Decision Date2003-11-07

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2003-11-07 under 510(k) number K032473. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE?

DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE is a medical device that received FDA 510(k) clearance on 2003-11-07. The listed applicant is Stryker Instruments. The 510(k) number is K032473.

When did DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE receive FDA 510(k) clearance?

DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE received FDA 510(k) clearance on 2003-11-07, under 510(k) number K032473.

Who is the listed applicant for DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE?

The FDA 510(k) record lists Stryker Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE?

The FDA product code for DEKOMPRESSOR PERCUTANEOUS DISCECTOMY PROBE is HRX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.