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FDA 510(k)

PRECISION SPINAL ADJUSTER MODEL 115

K-Number: K870910 · 1988-04-26

ApplicantKinetic Technology, Inc.
Decision Date1988-04-26
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

PRECISION SPINAL ADJUSTER MODEL 115 is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Technology, Inc.. It received FDA 510(k) clearance on 1988-04-26 under 510(k) number K870910. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION SPINAL ADJUSTER MODEL 115?

PRECISION SPINAL ADJUSTER MODEL 115 is a medical device that received FDA 510(k) clearance on 1988-04-26. The listed applicant is Kinetic Technology, Inc.. The 510(k) number is K870910.

When did PRECISION SPINAL ADJUSTER MODEL 115 receive FDA 510(k) clearance?

PRECISION SPINAL ADJUSTER MODEL 115 received FDA 510(k) clearance on 1988-04-26, under 510(k) number K870910.

Who is the listed applicant for PRECISION SPINAL ADJUSTER MODEL 115?

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

What is the FDA product code for PRECISION SPINAL ADJUSTER MODEL 115?

The FDA product code for PRECISION SPINAL ADJUSTER MODEL 115 is LXM.

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.

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Other records listing Kinetic Technology, 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.

K922694KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4K922695KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5K922692KINETIC TECHNOLOGY POCKET PRECISION ADJUSTORK922693KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1

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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