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FDA 510(k)

SILIMED CHIN IMPLANTS

K-Number: K981850 · 1998-07-09

ApplicantSilimed, LLC
Decision Date1998-07-09
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILIMED CHIN IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Silimed, LLC. It received FDA 510(k) clearance on 1998-07-09 under 510(k) number K981850. 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 SILIMED CHIN IMPLANTS?

SILIMED CHIN IMPLANTS is a medical device that received FDA 510(k) clearance on 1998-07-09. The listed applicant is Silimed, LLC. The 510(k) number is K981850.

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

SILIMED CHIN IMPLANTS received FDA 510(k) clearance on 1998-07-09, under 510(k) number K981850.

Who is the listed applicant for SILIMED CHIN IMPLANTS?

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

What is the FDA product code for SILIMED CHIN IMPLANTS?

The FDA product code for SILIMED CHIN IMPLANTS is FWP.

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Other records listing Silimed, LLC 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.

K981852SILIMED TISSUE EXPANDERK974479SILIMED VAGINAL STENTK981835SILIMED MALAR IMPLANTK981851SILIMED SILICONE CARVING BLOCKK981833SILIMED NASAL L SHAPED IMPLANTK980221SILIMED NASAL RETAINER

View all 9 devices →

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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