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FDA 510(k)

CHIN (MENTOPLASTY) IMPLANTS

K-Number: K831724 · 1983-08-12

ApplicantS. Jackson, Inc.
Decision Date1983-08-12
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHIN (MENTOPLASTY) IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is S. Jackson, Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K831724. 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 (MENTOPLASTY) IMPLANTS?

CHIN (MENTOPLASTY) IMPLANTS is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is S. Jackson, Inc.. The 510(k) number is K831724.

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

CHIN (MENTOPLASTY) IMPLANTS received FDA 510(k) clearance on 1983-08-12, under 510(k) number K831724.

Who is the listed applicant for CHIN (MENTOPLASTY) IMPLANTS?

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

What is the FDA product code for CHIN (MENTOPLASTY) IMPLANTS?

The FDA product code for CHIN (MENTOPLASTY) IMPLANTS is FWP.

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Other records listing S. Jackson, 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.

K080216SUPRAMESH EXTRAK973379STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETSK931613SUPRAMID SUTUREK931612NYLAMID SUTUREK931614MOPYLEN SUTUREK922630MOPYLEN

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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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