FDA 510(k)

MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY

K-Number: K922519 · 1994-03-29

Decision Date1994-03-29

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent for Some Indications

Device Summary

MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1994-03-29 under 510(k) number K922519. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY?

MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY is a medical device that received FDA 510(k) clearance on 1994-03-29. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K922519.

When did MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY receive FDA 510(k) clearance?

MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY received FDA 510(k) clearance on 1994-03-29, under 510(k) number K922519.

Who is the listed applicant for MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY?

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

What is the FDA product code for MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY?

The FDA product code for MOD. PERCUTANEOUS ARTHROSCOPIC MICRO DISCECTOMY 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.