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FDA 510(k)

CHIN IMPLANTS

K-Number: K760562 · 1976-11-02

ApplicantMediplast Laboratories, Inc.
Decision Date1976-11-02
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHIN IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Mediplast Laboratories, Inc.. It received FDA 510(k) clearance on 1976-11-02 under 510(k) number K760562. 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 CHIN IMPLANTS?

CHIN IMPLANTS is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is Mediplast Laboratories, Inc.. The 510(k) number is K760562.

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

CHIN IMPLANTS received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760562.

Who is the listed applicant for CHIN IMPLANTS?

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

What is the FDA product code for CHIN IMPLANTS?

The FDA product code for CHIN IMPLANTS is FWP.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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