FDA 510(k)

STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR

K-Number: K981717 · 1998-06-30

Decision Date1998-06-30

Product CodeFTD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 1998-06-30 under 510(k) number K981717. 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 ILLUMINATED RETRACTOR?

STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR is a medical device that received FDA 510(k) clearance on 1998-06-30. The listed applicant is Stryker Instruments. The 510(k) number is K981717.

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

STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR received FDA 510(k) clearance on 1998-06-30, under 510(k) number K981717.

Who is the listed applicant for STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR?

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, STRYKER ILLUMINATED RETRACTOR?

The FDA product code for STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR is 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.