FDA 510(k)

INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY

K-Number: K961713 · 1996-05-31

ApplicantKARL STORZ Endoscopy-America, Inc.

Decision Date1996-05-31

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1996-05-31 under 510(k) number K961713. 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 INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY?

INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY is a medical device that received FDA 510(k) clearance on 1996-05-31. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K961713.

When did INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY receive FDA 510(k) clearance?

INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY received FDA 510(k) clearance on 1996-05-31, under 510(k) number K961713.

Who is the listed applicant for INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY?

The FDA product code for INSTRUMENT SET FOR ARTHROSCOPIC PERCUTANEOUS DISCECTOMY is HRX.

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Other records listing KARL STORZ Endoscopy-America, Inc. as applicant

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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.