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FDA 510(k)

MAXISTAT PVA FOAM EMBOLIZATION PARTICLES

K-Number: K020033 · 2002-05-31

ApplicantSurgica Corp.
Decision Date2002-05-31
Product CodeHCG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MAXISTAT PVA FOAM EMBOLIZATION PARTICLES is the device name listed in this FDA 510(k) record. The listed applicant is Surgica Corp.. It received FDA 510(k) clearance on 2002-05-31 under 510(k) number K020033. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXISTAT PVA FOAM EMBOLIZATION PARTICLES?

MAXISTAT PVA FOAM EMBOLIZATION PARTICLES is a medical device that received FDA 510(k) clearance on 2002-05-31. The listed applicant is Surgica Corp.. The 510(k) number is K020033.

When did MAXISTAT PVA FOAM EMBOLIZATION PARTICLES receive FDA 510(k) clearance?

MAXISTAT PVA FOAM EMBOLIZATION PARTICLES received FDA 510(k) clearance on 2002-05-31, under 510(k) number K020033.

Who is the listed applicant for MAXISTAT PVA FOAM EMBOLIZATION PARTICLES?

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

What is the FDA product code for MAXISTAT PVA FOAM EMBOLIZATION PARTICLES?

The FDA product code for MAXISTAT PVA FOAM EMBOLIZATION PARTICLES is HCG.

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.

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Other records listing Surgica Corp. 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.

K032619MICROSTAT PVA FOAM EMBOLIZATION PARTICLESK001678PVA FOAM EMBOLIZATION PARTICLES

Related Devices (Code: HCG)

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.

K262419MICRUSFRAME (MFR100202); MICRUSFRAME (MFR100253); MICRUSFRAME (MFR100305); MICRUSFRAME (MFR100356); MICRUSFRAME (MFR100407); MICRUSFRAME (MFR100412); MICRUSFRAME (MFR100509); MICRUSFRAME (MFR100517); MICRUSFRAME (MFR100611); MICRUSFRAME (MFR100626); MICRUSFRAME (MFR100713); MICRUSFRAME (MFR100730); MICRUSFRAME (MFR100816); MICRUSFRAME (MFR100829); MICRUSFRAME (MFR140225); MICRUSFRAME (MFR140303); MICRUSFRAME (MFR140304); MICRUSFRAME (MFR140306); MICRUSFRAME (MFR140406); MICRUSFRAME (MFCerenovus, Inc.K261772Target Xtra Detachable CoilStryker NeurovscularK260351Numen™ Helia Coil Embolization System; NumenFR™ Detachment SystemMicroPort NeuroTech (Shanghai) Co., Ltd.K254221Optima Coil System (OptiOne Coil System)Balt USA, LLCK252694Target Detachable CoilStryker NeurovascularK251832InZone IST Detachment System; IZDS Connecting CableStryker Neurovascular

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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