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FDA 510(k)

STRYKER KNIFELIGHT

K-Number: K961122 · 1996-08-22

ApplicantStryker Instruments
Decision Date1996-08-22
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER KNIFELIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 1996-08-22 under 510(k) number K961122. The device is classified under product code FTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER KNIFELIGHT?

STRYKER KNIFELIGHT is a medical device that received FDA 510(k) clearance on 1996-08-22. The listed applicant is Stryker Instruments. The 510(k) number is K961122.

When did STRYKER KNIFELIGHT receive FDA 510(k) clearance?

STRYKER KNIFELIGHT received FDA 510(k) clearance on 1996-08-22, under 510(k) number K961122.

Who is the listed applicant for STRYKER KNIFELIGHT?

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

What is the FDA product code for STRYKER KNIFELIGHT?

The FDA product code for STRYKER KNIFELIGHT is FTD.

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Other records listing Stryker Instruments as applicant

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Related Devices (Code: FTD)

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.

K133425SCINTILLANT DUAL BENT TIP SURGICAL LIGHT, SCINTILLANT DUAL STRAIGHT TIP SURGICAL LIGHTEngineered Medical Solutions Co., LLCK130513VOLISTA 400; VOLISTA 600Maquet S.A.S.K123776POLARIS 100/200Drager Medical GmbHK111020ATRICURE DISSECTORAtriCure, Inc.K100234HM-LAMP IIHillusa, Inc.K100884STRYKER KNIFELIGHTHowmedica Osteonics Corp.

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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