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FDA 510(k)

HAND HELD ATLAS INSTRUMENT

K-Number: K955540 · 1996-03-04

ApplicantSpinalight, Inc.
Decision Date1996-03-04
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

HAND HELD ATLAS INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Spinalight, Inc.. It received FDA 510(k) clearance on 1996-03-04 under 510(k) number K955540. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAND HELD ATLAS INSTRUMENT?

HAND HELD ATLAS INSTRUMENT is a medical device that received FDA 510(k) clearance on 1996-03-04. The listed applicant is Spinalight, Inc.. The 510(k) number is K955540.

When did HAND HELD ATLAS INSTRUMENT receive FDA 510(k) clearance?

HAND HELD ATLAS INSTRUMENT received FDA 510(k) clearance on 1996-03-04, under 510(k) number K955540.

Who is the listed applicant for HAND HELD ATLAS INSTRUMENT?

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

What is the FDA product code for HAND HELD ATLAS INSTRUMENT?

The FDA product code for HAND HELD ATLAS INSTRUMENT is LXM.

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Other records listing Spinalight, 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.

K172536Atlas Percussion Adjusting InstrumentK001476TORQUE INSTRUMENT, MODEL 8500K946258MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENTK945954MODELS 4100 AND 4300 MULTITHERAPYK933622FLEXION DISTRACTION TABLEK933621HILO TABLE

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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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