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FDA 510(k)

ISO-ELASTIC CERCLAGE SYSTEM

K-Number: K030256 · 2003-10-21

ApplicantKinamed, Inc.
Decision Date2003-10-21
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ISO-ELASTIC CERCLAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Kinamed, Inc.. It received FDA 510(k) clearance on 2003-10-21 under 510(k) number K030256. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISO-ELASTIC CERCLAGE SYSTEM?

ISO-ELASTIC CERCLAGE SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-21. The listed applicant is Kinamed, Inc.. The 510(k) number is K030256.

When did ISO-ELASTIC CERCLAGE SYSTEM receive FDA 510(k) clearance?

ISO-ELASTIC CERCLAGE SYSTEM received FDA 510(k) clearance on 2003-10-21, under 510(k) number K030256.

Who is the listed applicant for ISO-ELASTIC CERCLAGE SYSTEM?

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

What is the FDA product code for ISO-ELASTIC CERCLAGE SYSTEM?

The FDA product code for ISO-ELASTIC CERCLAGE SYSTEM is JDQ.

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Other records listing Kinamed, Inc. as applicant

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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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