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FDA 510(k)

PERCUTANEOUS ENDOSCOPIC DISCECTOMY

K-Number: K960222 · 1996-03-08

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1996-03-08
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS ENDOSCOPIC DISCECTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1996-03-08 under 510(k) number K960222. 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 PERCUTANEOUS ENDOSCOPIC DISCECTOMY?

PERCUTANEOUS ENDOSCOPIC DISCECTOMY is a medical device that received FDA 510(k) clearance on 1996-03-08. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K960222.

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

PERCUTANEOUS ENDOSCOPIC DISCECTOMY received FDA 510(k) clearance on 1996-03-08, under 510(k) number K960222.

Who is the listed applicant for PERCUTANEOUS ENDOSCOPIC DISCECTOMY?

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

What is the FDA product code for PERCUTANEOUS ENDOSCOPIC DISCECTOMY?

The FDA product code for PERCUTANEOUS ENDOSCOPIC DISCECTOMY is HRX.

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Official Source

View on FDA Database →

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

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