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FDA 510(k)

STRAITH CHIN IMPLANTS

K-Number: K801073 · 1980-05-20

ApplicantSurgical Technology Laboratories, Inc.
Decision Date1980-05-20
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRAITH CHIN IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Technology Laboratories, Inc.. It received FDA 510(k) clearance on 1980-05-20 under 510(k) number K801073. The device is classified under product code FWP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRAITH CHIN IMPLANTS?

STRAITH CHIN IMPLANTS is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is Surgical Technology Laboratories, Inc.. The 510(k) number is K801073.

When did STRAITH CHIN IMPLANTS receive FDA 510(k) clearance?

STRAITH CHIN IMPLANTS received FDA 510(k) clearance on 1980-05-20, under 510(k) number K801073.

Who is the listed applicant for STRAITH CHIN IMPLANTS?

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

What is the FDA product code for STRAITH CHIN IMPLANTS?

The FDA product code for STRAITH CHIN IMPLANTS is FWP.

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Other records listing Surgical Technology Laboratories, 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.

K170582Saf-T-Vac Smoke and Fluid EvacuatorK021889SURGIFORM AUGMENTATION MATERIAL (S.F.A.M.)K983756SURGIFORM ANATOMICAL MALARK983755NASAL DORSAL SERIESK983754STANDARD CHINK964443SURGIFORM ANATOMICAL MALAR

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Related Devices (Code: FWP)

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.

K254233MEDPOR Customized Implant KitStryker Leibinger GmbH & Co KGK232593FITme Customized Silicone ImplantKeosan Trading Co.K200610Customized Contour ImplantImplantech Associates, Inc.K191130Customized Contour ImplantImplantech Associates, Inc.K191916Stryker CMF MEDPOR Priority Customized Implant KitStryker Leibinger GmbH & Co KGK153508Stryker CMF MEDPOR Customized ImplantStryker

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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