Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SILIMED PECTORAL IMPLANT

K-Number: K042054 · 2005-02-23

ApplicantSilimed, Inc.
Decision Date2005-02-23
Product CodeMIB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SILIMED PECTORAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Silimed, Inc.. It received FDA 510(k) clearance on 2005-02-23 under 510(k) number K042054. The device is classified under product code MIB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILIMED PECTORAL IMPLANT?

SILIMED PECTORAL IMPLANT is a medical device that received FDA 510(k) clearance on 2005-02-23. The listed applicant is Silimed, Inc.. The 510(k) number is K042054.

When did SILIMED PECTORAL IMPLANT receive FDA 510(k) clearance?

SILIMED PECTORAL IMPLANT received FDA 510(k) clearance on 2005-02-23, under 510(k) number K042054.

Who is the listed applicant for SILIMED PECTORAL IMPLANT?

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

What is the FDA product code for SILIMED PECTORAL IMPLANT?

The FDA product code for SILIMED PECTORAL IMPLANT is MIB.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: MIB)

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.

K241150MISTI Silicone ImplantKeosan Trading Co.K223051Pre-Formed Silicone BlockInternational Medical Devices, Inc.K222748ShiNeo Silicone ImplantShineo Technology Co., Ltd.K200073AugMENTA Penile ImplantAugmenta, LLCK220760Pre-Formed Penile Silicone BlockInternational Medical Devices, Inc.K193392BioSiCar Silicone ImplantMetalware Technology Corp.

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.

↑