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FDA 510(k)

AXON MP-1 MICROPOSITIONER

K-Number: K990683 · 1999-11-03

ApplicantAxon Instruments, Inc.
Decision Date1999-11-03
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AXON MP-1 MICROPOSITIONER is the device name listed in this FDA 510(k) record. The listed applicant is Axon Instruments, Inc.. It received FDA 510(k) clearance on 1999-11-03 under 510(k) number K990683. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXON MP-1 MICROPOSITIONER?

AXON MP-1 MICROPOSITIONER is a medical device that received FDA 510(k) clearance on 1999-11-03. The listed applicant is Axon Instruments, Inc.. The 510(k) number is K990683.

When did AXON MP-1 MICROPOSITIONER receive FDA 510(k) clearance?

AXON MP-1 MICROPOSITIONER received FDA 510(k) clearance on 1999-11-03, under 510(k) number K990683.

Who is the listed applicant for AXON MP-1 MICROPOSITIONER?

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

What is the FDA product code for AXON MP-1 MICROPOSITIONER?

The FDA product code for AXON MP-1 MICROPOSITIONER is HAW.

Related Clinical Trials

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Other records listing Axon Instruments, 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.

K970943GUIDELINE SYSTEMK971318MM-1 MOVEMENT MONITOR

Related Devices (Code: HAW)

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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.

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