FDA 510(k)

MANIFOLD WITH EXTENSION SET

K-Number: K982368 · 1998-07-31

Decision Date1998-07-31

Product CodeFMG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MANIFOLD WITH EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Cross Intl.. It received FDA 510(k) clearance on 1998-07-31 under 510(k) number K982368. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANIFOLD WITH EXTENSION SET?

MANIFOLD WITH EXTENSION SET is a medical device that received FDA 510(k) clearance on 1998-07-31. The listed applicant is Interpore Cross Intl.. The 510(k) number is K982368.

When did MANIFOLD WITH EXTENSION SET receive FDA 510(k) clearance?

MANIFOLD WITH EXTENSION SET received FDA 510(k) clearance on 1998-07-31, under 510(k) number K982368.

Who is the listed applicant for MANIFOLD WITH EXTENSION SET?

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

What is the FDA product code for MANIFOLD WITH EXTENSION SET?

The FDA product code for MANIFOLD WITH EXTENSION SET is FMG.

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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.