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FDA 510(k)

MEDPOR CONTAIN CAN IMPLANT

K-Number: K102184 · 2011-01-07

ApplicantPorex Surgical, Inc.
Decision Date2011-01-07
Product CodeNPK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEDPOR CONTAIN CAN IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Porex Surgical, Inc.. It received FDA 510(k) clearance on 2011-01-07 under 510(k) number K102184. The device is classified under product code NPK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDPOR CONTAIN CAN IMPLANT?

MEDPOR CONTAIN CAN IMPLANT is a medical device that received FDA 510(k) clearance on 2011-01-07. The listed applicant is Porex Surgical, Inc.. The 510(k) number is K102184.

When did MEDPOR CONTAIN CAN IMPLANT receive FDA 510(k) clearance?

MEDPOR CONTAIN CAN IMPLANT received FDA 510(k) clearance on 2011-01-07, under 510(k) number K102184.

Who is the listed applicant for MEDPOR CONTAIN CAN IMPLANT?

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

What is the FDA product code for MEDPOR CONTAIN CAN IMPLANT?

The FDA product code for MEDPOR CONTAIN CAN IMPLANT is NPK.

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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.

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Other records listing Porex Surgical, 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.

K101835MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079K091807MEDPOR FIXATION SYSTEMK091120MEDPOR CONTAIN IMPLANTK083621MEDPOR CUSTOMIZED SURGICAL IMPLANTK071335MEDPOR ATTRACTOR IMPLANTK052297POREX ELECTROSURGERY NEEDLE

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Related Devices (Code: NPK)

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.

K221851Lumina-PTFE TitaniumCriteria Industria E Comercio DE Produtos MedicinaisK222549OpenTexPurgo Biologics, Inc.K211554InnoGenic Non-resorbable MembraneCowellmedi Co., Ltd.K210797Bio-MEM Ti Reinforced MembraneB&Medi Co., Ltd.K201187Cytoplast Titanium-Reinforced PTFE MembranesOsteogenics Biomedical, Inc.K171774RPM Reinforced PTFE MeshOsteogenics Biomedical, Inc.

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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