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FDA 510(k)

ANTERIORS AND POSTERIORS, PLASTIC

K-Number: K780217 · 1978-03-15

Decision Date1978-03-15
Product CodeELM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANTERIORS AND POSTERIORS, PLASTIC is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1978-03-15 under 510(k) number K780217. The device is classified under product code ELM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTERIORS AND POSTERIORS, PLASTIC?

ANTERIORS AND POSTERIORS, PLASTIC is a medical device that received FDA 510(k) clearance on 1978-03-15. The listed applicant is Dentsply Intl.. The 510(k) number is K780217.

When did ANTERIORS AND POSTERIORS, PLASTIC receive FDA 510(k) clearance?

ANTERIORS AND POSTERIORS, PLASTIC received FDA 510(k) clearance on 1978-03-15, under 510(k) number K780217.

Who is the listed applicant for ANTERIORS AND POSTERIORS, PLASTIC?

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 ANTERIORS AND POSTERIORS, PLASTIC?

The FDA product code for ANTERIORS AND POSTERIORS, PLASTIC is ELM.

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: ELM)

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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