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FDA 510(k)

POREX(TM) MALAR IMPLANT

K-Number: K870182 · 1987-02-24

ApplicantPorex Medical
Decision Date1987-02-24
Product Code
DecisionSubstantially Equivalent

Device Summary

POREX(TM) MALAR IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Porex Medical. It received FDA 510(k) clearance on 1987-02-24 under 510(k) number K870182. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POREX(TM) MALAR IMPLANT?

POREX(TM) MALAR IMPLANT is a medical device that received FDA 510(k) clearance on 1987-02-24. The listed applicant is Porex Medical. The 510(k) number is K870182.

When did POREX(TM) MALAR IMPLANT receive FDA 510(k) clearance?

POREX(TM) MALAR IMPLANT received FDA 510(k) clearance on 1987-02-24, under 510(k) number K870182.

Who is the listed applicant for POREX(TM) MALAR IMPLANT?

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

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 Porex Medical 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.

K872791POREX NERVE LOCATORK873044POREX OTOLOGY INSTRUMENTSK872947POREX QUALITY PLASTIC SURGERY INSTRUMENTSK863946POREX(TM) EXTRA-OCULAR ORBITAL IMPLANTK863943POREX(TM) EYE SPHERE IMPLANTK870257POREX(TM) SILICONE SURGICAL IMPLANTS FOR E.N.T.

View all 15 devices →

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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