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FDA 510(k)

MEDPOR OCULAR SCREW AND ACCEOSSORIES

K-Number: K971583 · 1997-06-30

ApplicantPorex Technologies Corp.
Decision Date1997-06-30
Product CodeMQU
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MEDPOR OCULAR SCREW AND ACCEOSSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Porex Technologies Corp.. It received FDA 510(k) clearance on 1997-06-30 under 510(k) number K971583. The device is classified under product code MQU. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDPOR OCULAR SCREW AND ACCEOSSORIES?

MEDPOR OCULAR SCREW AND ACCEOSSORIES is a medical device that received FDA 510(k) clearance on 1997-06-30. The listed applicant is Porex Technologies Corp.. The 510(k) number is K971583.

When did MEDPOR OCULAR SCREW AND ACCEOSSORIES receive FDA 510(k) clearance?

MEDPOR OCULAR SCREW AND ACCEOSSORIES received FDA 510(k) clearance on 1997-06-30, under 510(k) number K971583.

Who is the listed applicant for MEDPOR OCULAR SCREW AND ACCEOSSORIES?

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

What is the FDA product code for MEDPOR OCULAR SCREW AND ACCEOSSORIES?

The FDA product code for MEDPOR OCULAR SCREW AND ACCEOSSORIES is MQU.

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 Technologies 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.

K922489MEDPOR SURG IMPLANT MATERIAL:PREFOR CRAN/FAC IMPLA

Related Devices (Code: MQU)

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.

K000151PERRY-KOLBERG (PK) HA-COATED TITANIUM SLEEVEIntegrated Orbital Implants, Inc.K980822TITANIUM PEG SYSTEMFci Ophthalmics, Inc.K974203PERRY-KOLBERG (PK) TITANIUM MOTILITY/SUPPORT SYSTEMIntegrated Orbital Implants, 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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