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FDA 510(k)

DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE

K-Number: K013513 · 2002-01-17

ApplicantPain Concepts, Inc.
Decision Date2002-01-17
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Pain Concepts, Inc.. It received FDA 510(k) clearance on 2002-01-17 under 510(k) number K013513. 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 LUMBAR DISCECTOMY PROBE?

DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE is a medical device that received FDA 510(k) clearance on 2002-01-17. The listed applicant is Pain Concepts, Inc.. The 510(k) number is K013513.

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

DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE received FDA 510(k) clearance on 2002-01-17, under 510(k) number K013513.

Who is the listed applicant for DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE?

The FDA 510(k) record lists Pain Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Related Devices (Code: HRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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