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FDA 510(k)

MEDPOR ATTRACTOR IMPLANT

K-Number: K071335 · 2007-08-08

ApplicantPorex Surgical, Inc.
Decision Date2007-08-08
Product CodeHPZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MEDPOR ATTRACTOR 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 2007-08-08 under 510(k) number K071335. The device is classified under product code HPZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDPOR ATTRACTOR IMPLANT?

MEDPOR ATTRACTOR IMPLANT is a medical device that received FDA 510(k) clearance on 2007-08-08. The listed applicant is Porex Surgical, Inc.. The 510(k) number is K071335.

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

MEDPOR ATTRACTOR IMPLANT received FDA 510(k) clearance on 2007-08-08, under 510(k) number K071335.

Who is the listed applicant for MEDPOR ATTRACTOR 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 ATTRACTOR IMPLANT?

The FDA product code for MEDPOR ATTRACTOR IMPLANT is HPZ.

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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.

K102184MEDPOR CONTAIN CAN IMPLANTK101835MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079K091807MEDPOR FIXATION SYSTEMK091120MEDPOR CONTAIN IMPLANTK083621MEDPOR CUSTOMIZED SURGICAL IMPLANTK052297POREX ELECTROSURGERY NEEDLE

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Related Devices (Code: HPZ)

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.

K212741EZYPORFci (France Chirurgie Instrumentation) SasK123764DURETTE OCULAR IMPLANTOculo-Plastik, Inc.K110554BIOCERAMIC ORBITAL IMPLANT, ORBTEXCeramisys, Ltd.K112176SILICONE SPHERESOculo Plastik, Inc.K083342ORBITAL RECONSTRUCTIVE IMPLANT IIEvera Medical, Inc.K082850EYE SPHERESProduct and Educational Services, LLC

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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