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FDA 510(k)

STRYKER T4 HYTREL ZIPPER TOGA

K-Number: K040764 · 2004-04-27

ApplicantStryker Corp.
Decision Date2004-04-27
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER T4 HYTREL ZIPPER TOGA is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2004-04-27 under 510(k) number K040764. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER T4 HYTREL ZIPPER TOGA?

STRYKER T4 HYTREL ZIPPER TOGA is a medical device that received FDA 510(k) clearance on 2004-04-27. The listed applicant is Stryker Corp.. The 510(k) number is K040764.

When did STRYKER T4 HYTREL ZIPPER TOGA receive FDA 510(k) clearance?

STRYKER T4 HYTREL ZIPPER TOGA received FDA 510(k) clearance on 2004-04-27, under 510(k) number K040764.

Who is the listed applicant for STRYKER T4 HYTREL ZIPPER TOGA?

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

What is the FDA product code for STRYKER T4 HYTREL ZIPPER TOGA?

The FDA product code for STRYKER T4 HYTREL ZIPPER TOGA is FYA.

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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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