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FDA 510(k)

MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES

K-Number: K904950 · 1990-11-26

ApplicantLeander Research, Mfg & Distr., Inc.
Decision Date1990-11-26
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES is the device name listed in this FDA 510(k) record. The listed applicant is Leander Research, Mfg & Distr., Inc.. It received FDA 510(k) clearance on 1990-11-26 under 510(k) number K904950. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES?

MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES is a medical device that received FDA 510(k) clearance on 1990-11-26. The listed applicant is Leander Research, Mfg & Distr., Inc.. The 510(k) number is K904950.

When did MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES receive FDA 510(k) clearance?

MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES received FDA 510(k) clearance on 1990-11-26, under 510(k) number K904950.

Who is the listed applicant for MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES?

The FDA 510(k) record lists Leander Research, Mfg & Distr., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES?

The FDA product code for MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES is INQ.

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Related Devices (Code: INQ)

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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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