FDA 510(k)

SPINAL NEEDLE

K-Number: K880812 · 1988-03-11

ApplicantT. Korossurgical Instruments Corp.

Decision Date1988-03-11

Product CodeGDM

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SPINAL NEEDLE 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 1988-03-11 under 510(k) number K880812. The device is classified under product code GDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINAL NEEDLE?

SPINAL NEEDLE is a medical device that received FDA 510(k) clearance on 1988-03-11. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K880812.

When did SPINAL NEEDLE receive FDA 510(k) clearance?

SPINAL NEEDLE received FDA 510(k) clearance on 1988-03-11, under 510(k) number K880812.

Who is the listed applicant for SPINAL NEEDLE?

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 SPINAL NEEDLE?

The FDA product code for SPINAL NEEDLE is GDM.

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Other records listing T. Korossurgical Instruments Corp. as applicant

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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.