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FDA 510(k)

STRYKER TRAUMA TRAY

K-Number: K894470 · 1989-08-18

ApplicantStryker Corp.
Decision Date1989-08-18
Product CodeKYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER TRAUMA TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1989-08-18 under 510(k) number K894470. The device is classified under product code KYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER TRAUMA TRAY?

STRYKER TRAUMA TRAY is a medical device that received FDA 510(k) clearance on 1989-08-18. The listed applicant is Stryker Corp.. The 510(k) number is K894470.

When did STRYKER TRAUMA TRAY receive FDA 510(k) clearance?

STRYKER TRAUMA TRAY received FDA 510(k) clearance on 1989-08-18, under 510(k) number K894470.

Who is the listed applicant for STRYKER TRAUMA TRAY?

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 TRAUMA TRAY?

The FDA product code for STRYKER TRAUMA TRAY is KYZ.

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Other records listing Stryker 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.

K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122284HOFFMANN 3K122053SHAPEMATCH CUTTING GUIDE

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Related Devices (Code: KYZ)

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.

K201877OtoSet- Ear Cleaning SystemSafkan, Inc.K102563SINGLE CANNULA EXTENDED APPLICATORMicromedics, Inc.K092022TISSU TRANS HARVEST TUBINGShippert Medical Technologies Corp.K050797TISSU-TRANSShippert Medical Technologies Corp.K991254QS DELIVERY SYSTEMSub-Q, Inc.K982435IRRIGATION SYRINGE KITSub-Q, 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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