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FDA 510(k)

EVERSTICK POST

K-Number: K030820 · 2003-05-20

ApplicantStick Tech , Ltd.
Decision Date2003-05-20
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EVERSTICK POST is the device name listed in this FDA 510(k) record. The listed applicant is Stick Tech , Ltd.. It received FDA 510(k) clearance on 2003-05-20 under 510(k) number K030820. The device is classified under product code ELR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVERSTICK POST?

EVERSTICK POST is a medical device that received FDA 510(k) clearance on 2003-05-20. The listed applicant is Stick Tech , Ltd.. The 510(k) number is K030820.

When did EVERSTICK POST receive FDA 510(k) clearance?

EVERSTICK POST received FDA 510(k) clearance on 2003-05-20, under 510(k) number K030820.

Who is the listed applicant for EVERSTICK POST?

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

What is the FDA product code for EVERSTICK POST?

The FDA product code for EVERSTICK POST is ELR.

Related Clinical Trials

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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Other records listing Stick Tech , Ltd. 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.

K051953EVERSTICK A&OK031341STICK FLOWK030072EVERSTICK PERIOK021126EVERSTICK ORTHOK011799EVERSTICKNETK011788EVERSTICK

View all 9 devices →

Related Devices (Code: ELR)

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.

K060075FIBER-METAL POSTForemost Dental, LLCK042848FRC POSTEC PLUSIvoclar Vivadent, Inc.K020431FIBIOCOREEst. AnthogyrK012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, Inc.K012849GLASS POSTJ. Morita USA, Inc.

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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