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FDA 510(k)

ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE

K-Number: K802975 · 1981-01-14

Decision Date1981-01-14
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1981-01-14 under 510(k) number K802975. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE?

ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE is a medical device that received FDA 510(k) clearance on 1981-01-14. The listed applicant is Dentsply Intl.. The 510(k) number is K802975.

When did ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE receive FDA 510(k) clearance?

ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE received FDA 510(k) clearance on 1981-01-14, under 510(k) number K802975.

Who is the listed applicant for ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE?

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

What is the FDA product code for ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE?

The FDA product code for ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE is EBF.

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.

Other records listing Dentsply Intl. 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.

View all 279 devices →

Related Devices (Code: EBF)

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.

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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