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FDA 510(k)

ACTIVATOR V SPINAL ADJUSTING INSTRUMENT

K-Number: K072519 · 2007-10-23

ApplicantActivator Methods International, Ltd.
Decision Date2007-10-23
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

ACTIVATOR V SPINAL ADJUSTING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Activator Methods International, Ltd.. It received FDA 510(k) clearance on 2007-10-23 under 510(k) number K072519. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIVATOR V SPINAL ADJUSTING INSTRUMENT?

ACTIVATOR V SPINAL ADJUSTING INSTRUMENT is a medical device that received FDA 510(k) clearance on 2007-10-23. The listed applicant is Activator Methods International, Ltd.. The 510(k) number is K072519.

When did ACTIVATOR V SPINAL ADJUSTING INSTRUMENT receive FDA 510(k) clearance?

ACTIVATOR V SPINAL ADJUSTING INSTRUMENT received FDA 510(k) clearance on 2007-10-23, under 510(k) number K072519.

Who is the listed applicant for ACTIVATOR V SPINAL ADJUSTING INSTRUMENT?

The FDA 510(k) record lists Activator Methods International, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTIVATOR V SPINAL ADJUSTING INSTRUMENT?

The FDA product code for ACTIVATOR V SPINAL ADJUSTING INSTRUMENT is LXM.

Related Clinical Trials

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Other records listing Activator Methods International, Ltd. 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.

K112606ACTIVATOR V-EK003185FS ACTIVATOR III

Related Devices (Code: LXM)

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.

K234036SONIK MONARK 100Neuro Spinal Innovation, Inc.K192629SpinalyticsOptima Health Solutions International Corp.K172536Atlas Percussion Adjusting InstrumentSpinalight, Inc.K160278VSTAAR AdjusteRSpinal Acoustics, LLCK112606ACTIVATOR V-EActivator Methods International, Ltd.K082218MAX ADJUSTING INSTRUMENTManna Omni International, Inc.

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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