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FDA 510(k)

POLYVAC INSTRUMENT DELIVERY SYSTEM

K-Number: K040223 · 2004-10-22

ApplicantSymmetry Medical USA, Inc.
Decision Date2004-10-22
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POLYVAC INSTRUMENT DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Symmetry Medical USA, Inc.. It received FDA 510(k) clearance on 2004-10-22 under 510(k) number K040223. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYVAC INSTRUMENT DELIVERY SYSTEM?

POLYVAC INSTRUMENT DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2004-10-22. The listed applicant is Symmetry Medical USA, Inc.. The 510(k) number is K040223.

When did POLYVAC INSTRUMENT DELIVERY SYSTEM receive FDA 510(k) clearance?

POLYVAC INSTRUMENT DELIVERY SYSTEM received FDA 510(k) clearance on 2004-10-22, under 510(k) number K040223.

Who is the listed applicant for POLYVAC INSTRUMENT DELIVERY SYSTEM?

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

What is the FDA product code for POLYVAC INSTRUMENT DELIVERY SYSTEM?

The FDA product code for POLYVAC INSTRUMENT DELIVERY SYSTEM is KCT.

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Related Devices (Code: KCT)

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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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