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FDA 510(k)

REUSABLE DEXTRA SYNOVIAL RESECTORS IN 3.5/4.5/5.5M

K-Number: K853491 · 1985-09-06

ApplicantChattanooga Group, Inc.
Decision Date1985-09-06
Product Code
DecisionSubstantially Equivalent

Device Summary

REUSABLE DEXTRA SYNOVIAL RESECTORS IN 3.5/4.5/5.5M 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 1985-09-06 under 510(k) number K853491. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE DEXTRA SYNOVIAL RESECTORS IN 3.5/4.5/5.5M?

REUSABLE DEXTRA SYNOVIAL RESECTORS IN 3.5/4.5/5.5M is a medical device that received FDA 510(k) clearance on 1985-09-06. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K853491.

When did REUSABLE DEXTRA SYNOVIAL RESECTORS IN 3.5/4.5/5.5M receive FDA 510(k) clearance?

REUSABLE DEXTRA SYNOVIAL RESECTORS IN 3.5/4.5/5.5M received FDA 510(k) clearance on 1985-09-06, under 510(k) number K853491.

Who is the listed applicant for REUSABLE DEXTRA SYNOVIAL RESECTORS IN 3.5/4.5/5.5M?

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

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Other records listing Chattanooga Group, Inc. as applicant

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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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