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FDA 510(k)

CHIN IMPLANT STYLE I

K-Number: K945998 · 1995-02-07

ApplicantKing & Spalding
Decision Date1995-02-07
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHIN IMPLANT STYLE I is the device name listed in this FDA 510(k) record. The listed applicant is King & Spalding. It received FDA 510(k) clearance on 1995-02-07 under 510(k) number K945998. 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 IMPLANT STYLE I?

CHIN IMPLANT STYLE I is a medical device that received FDA 510(k) clearance on 1995-02-07. The listed applicant is King & Spalding. The 510(k) number is K945998.

When did CHIN IMPLANT STYLE I receive FDA 510(k) clearance?

CHIN IMPLANT STYLE I received FDA 510(k) clearance on 1995-02-07, under 510(k) number K945998.

Who is the listed applicant for CHIN IMPLANT STYLE I?

The FDA 510(k) record lists King & Spalding as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHIN IMPLANT STYLE I?

The FDA product code for CHIN IMPLANT STYLE I is FWP.

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Other records listing King & Spalding 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.

K942423NAIS WRIST BLOOD PRESSURE METERK942422PANASONIC WRIST BLOOD PRESSURE METERK944408IMPLANTECH MEDICAL GRADE SILICONE SHEETINGK942420IMPLANTECH MIDFACE-SUBMALAR LE FORT IMPLANTK942421IMPLANTECH LATERAL MANDIBULAR BAR IMPLANTK941972HEMO-O-LOK

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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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