FDA 510(k)

AMSEN POSTERIOR DISC EVACUATOR

K-Number: K921643 · 1992-06-03

Decision Date1992-06-03

Product CodeLXH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

AMSEN POSTERIOR DISC EVACUATOR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Med/Surg, Inc.. It received FDA 510(k) clearance on 1992-06-03 under 510(k) number K921643. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSEN POSTERIOR DISC EVACUATOR?

AMSEN POSTERIOR DISC EVACUATOR is a medical device that received FDA 510(k) clearance on 1992-06-03. The listed applicant is Advanced Med/Surg, Inc.. The 510(k) number is K921643.

When did AMSEN POSTERIOR DISC EVACUATOR receive FDA 510(k) clearance?

AMSEN POSTERIOR DISC EVACUATOR received FDA 510(k) clearance on 1992-06-03, under 510(k) number K921643.

Who is the listed applicant for AMSEN POSTERIOR DISC EVACUATOR?

The FDA 510(k) record lists Advanced Med/Surg, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMSEN POSTERIOR DISC EVACUATOR?

The FDA product code for AMSEN POSTERIOR DISC EVACUATOR is LXH.

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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.