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FDA 510(k)

STRYKER KNIFELIGHT

K-Number: K100884 · 2010-06-25

ApplicantHowmedica Osteonics Corp.
Decision Date2010-06-25
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 Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2010-06-25 under 510(k) number K100884. 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 2010-06-25. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K100884.

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

STRYKER KNIFELIGHT received FDA 510(k) clearance on 2010-06-25, under 510(k) number K100884.

Who is the listed applicant for STRYKER KNIFELIGHT?

The FDA 510(k) record lists Howmedica Osteonics Corp. 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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Related Devices (Code: FTD)

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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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