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FDA 510(k)

QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H

K-Number: K002390 · 2000-11-02

ApplicantLsi Intl., Inc.
Decision Date2000-11-02
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H is the device name listed in this FDA 510(k) record. The listed applicant is Lsi Intl., Inc.. It received FDA 510(k) clearance on 2000-11-02 under 510(k) number K002390. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H?

QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H is a medical device that received FDA 510(k) clearance on 2000-11-02. The listed applicant is Lsi Intl., Inc.. The 510(k) number is K002390.

When did QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H receive FDA 510(k) clearance?

QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H received FDA 510(k) clearance on 2000-11-02, under 510(k) number K002390.

Who is the listed applicant for QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H?

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

What is the FDA product code for QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H?

The FDA product code for QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H is JFB.

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Other records listing Lsi Intl., 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.

K984021MS300K984113MS400K970696S.P. 100K933653MS 2500

Related Devices (Code: JFB)

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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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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