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FDA 510(k)

IST-200 INTERSEGMENTAL TRACTION TABLE

K-Number: K900304 · 1990-04-11

ApplicantChattanooga Group, Inc.
Decision Date1990-04-11
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IST-200 INTERSEGMENTAL TRACTION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1990-04-11 under 510(k) number K900304. 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 IST-200 INTERSEGMENTAL TRACTION TABLE?

IST-200 INTERSEGMENTAL TRACTION TABLE is a medical device that received FDA 510(k) clearance on 1990-04-11. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K900304.

When did IST-200 INTERSEGMENTAL TRACTION TABLE receive FDA 510(k) clearance?

IST-200 INTERSEGMENTAL TRACTION TABLE received FDA 510(k) clearance on 1990-04-11, under 510(k) number K900304.

Who is the listed applicant for IST-200 INTERSEGMENTAL TRACTION TABLE?

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

What is the FDA product code for IST-200 INTERSEGMENTAL TRACTION TABLE?

The FDA product code for IST-200 INTERSEGMENTAL TRACTION TABLE is JFB.

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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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