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FDA 510(k)

MEDPOR PTERIONAL SURGICAL IMPLANT

K-Number: K002586 · 2000-11-17

ApplicantPorex Surgical Products Group
Decision Date2000-11-17
Product CodeMNF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDPOR PTERIONAL SURGICAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Porex Surgical Products Group. It received FDA 510(k) clearance on 2000-11-17 under 510(k) number K002586. The device is classified under product code MNF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDPOR PTERIONAL SURGICAL IMPLANT?

MEDPOR PTERIONAL SURGICAL IMPLANT is a medical device that received FDA 510(k) clearance on 2000-11-17. The listed applicant is Porex Surgical Products Group. The 510(k) number is K002586.

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

MEDPOR PTERIONAL SURGICAL IMPLANT received FDA 510(k) clearance on 2000-11-17, under 510(k) number K002586.

Who is the listed applicant for MEDPOR PTERIONAL SURGICAL IMPLANT?

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

What is the FDA product code for MEDPOR PTERIONAL SURGICAL IMPLANT?

The FDA product code for MEDPOR PTERIONAL SURGICAL IMPLANT is MNF.

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Related Devices (Code: MNF)

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.

K111069OSTEOSYMBIONICS, ST TEMPORALIS IMPLANTOsteosymbionics, 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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