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FDA 510(k)

DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM

K-Number: K870130 · 1987-02-19

ApplicantDen-Mat Corp.
Decision Date1987-02-19
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Den-Mat Corp.. It received FDA 510(k) clearance on 1987-02-19 under 510(k) number K870130. 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 DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM?

DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM is a medical device that received FDA 510(k) clearance on 1987-02-19. The listed applicant is Den-Mat Corp.. The 510(k) number is K870130.

When did DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM receive FDA 510(k) clearance?

DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM received FDA 510(k) clearance on 1987-02-19, under 510(k) number K870130.

Who is the listed applicant for DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM?

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

What is the FDA product code for DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM?

The FDA product code for DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM is ELR.

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Other records listing Den-Mat Corp. 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.

K9831061ST IMPRESSIONK895731DEN-MAT CERINATE PORCELAINK895269DEN-MAT LAMI-QUICKK881918LIGHT-CURED ZIONOMER CEMENTK875351DEN-MAT PORETCH (PORCELAIN ETCHANT)K872510DEN-MAT TENURE

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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.K030820EVERSTICK POSTStick Tech , Ltd.K020431FIBIOCOREEst. AnthogyrK012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, 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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