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FDA 510(k)

AMSEN HOCKEY STICK CHISEL

K-Number: K921644 · 1992-06-03

Decision Date1992-06-03
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AMSEN HOCKEY STICK CHISEL 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 K921644. 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 HOCKEY STICK CHISEL?

AMSEN HOCKEY STICK CHISEL 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 K921644.

When did AMSEN HOCKEY STICK CHISEL receive FDA 510(k) clearance?

AMSEN HOCKEY STICK CHISEL received FDA 510(k) clearance on 1992-06-03, under 510(k) number K921644.

Who is the listed applicant for AMSEN HOCKEY STICK CHISEL?

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 HOCKEY STICK CHISEL?

The FDA product code for AMSEN HOCKEY STICK CHISEL is LXH.

Related Clinical Trials

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.

Other records listing Advanced Med/Surg, Inc. as applicant

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.

View all 10 devices →

Related Devices (Code: LXH)

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.

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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