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FDA 510(k)

ENDOSSEOUS IMPLANTS

K-Number: K904236 · 1991-11-27

ApplicantAttachments Intl., Inc.
Decision Date1991-11-27
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOSSEOUS IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Attachments Intl., Inc.. It received FDA 510(k) clearance on 1991-11-27 under 510(k) number K904236. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSSEOUS IMPLANTS?

ENDOSSEOUS IMPLANTS is a medical device that received FDA 510(k) clearance on 1991-11-27. The listed applicant is Attachments Intl., Inc.. The 510(k) number is K904236.

When did ENDOSSEOUS IMPLANTS receive FDA 510(k) clearance?

ENDOSSEOUS IMPLANTS received FDA 510(k) clearance on 1991-11-27, under 510(k) number K904236.

Who is the listed applicant for ENDOSSEOUS IMPLANTS?

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

What is the FDA product code for ENDOSSEOUS IMPLANTS?

The FDA product code for ENDOSSEOUS IMPLANTS is DZE.

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Other records listing Attachments Intl., Inc. 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.

K900099THE O-RING SYSTEM - ORS

Related Devices (Code: DZE)

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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Official Source

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