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FDA 510(k)

INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS

K-Number: K072454 · 2007-10-16

ApplicantIntegra Radionics, Inc.
Decision Date2007-10-16
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS is the device name listed in this FDA 510(k) record. The listed applicant is Integra Radionics, Inc.. It received FDA 510(k) clearance on 2007-10-16 under 510(k) number K072454. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS?

INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS is a medical device that received FDA 510(k) clearance on 2007-10-16. The listed applicant is Integra Radionics, Inc.. The 510(k) number is K072454.

When did INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS receive FDA 510(k) clearance?

INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS received FDA 510(k) clearance on 2007-10-16, under 510(k) number K072454.

Who is the listed applicant for INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS?

The FDA 510(k) record lists Integra Radionics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS?

The FDA product code for INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS is IYE.

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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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