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FDA 510(k)

SMISSON STABILIZATION SYSTEM

K-Number: K021979 · 2003-06-27

ApplicantSmisson-Cartledge
Decision Date2003-06-27
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SMISSON STABILIZATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Smisson-Cartledge. It received FDA 510(k) clearance on 2003-06-27 under 510(k) number K021979. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMISSON STABILIZATION SYSTEM?

SMISSON STABILIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 2003-06-27. The listed applicant is Smisson-Cartledge. The 510(k) number is K021979.

When did SMISSON STABILIZATION SYSTEM receive FDA 510(k) clearance?

SMISSON STABILIZATION SYSTEM received FDA 510(k) clearance on 2003-06-27, under 510(k) number K021979.

Who is the listed applicant for SMISSON STABILIZATION SYSTEM?

The FDA 510(k) record lists Smisson-Cartledge as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMISSON STABILIZATION SYSTEM?

The FDA product code for SMISSON STABILIZATION SYSTEM is KWQ.

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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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