FDA 510(k)

FLUTED SUCTION MENISCAL CUTTER

K-Number: K850789 · 1985-06-28

ApplicantT. Korossurgical Instruments Corp.

Decision Date1985-06-28

Product CodeKIJ

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

FLUTED SUCTION MENISCAL CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is T. Korossurgical Instruments Corp.. It received FDA 510(k) clearance on 1985-06-28 under 510(k) number K850789. The device is classified under product code KIJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUTED SUCTION MENISCAL CUTTER?

FLUTED SUCTION MENISCAL CUTTER is a medical device that received FDA 510(k) clearance on 1985-06-28. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K850789.

When did FLUTED SUCTION MENISCAL CUTTER receive FDA 510(k) clearance?

FLUTED SUCTION MENISCAL CUTTER received FDA 510(k) clearance on 1985-06-28, under 510(k) number K850789.

Who is the listed applicant for FLUTED SUCTION MENISCAL CUTTER?

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

What is the FDA product code for FLUTED SUCTION MENISCAL CUTTER?

The FDA product code for FLUTED SUCTION MENISCAL CUTTER is KIJ.

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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.