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FDA 510(k)

THE COBALT SCALPEL

K-Number: K960892 · 1996-06-03

ApplicantNova Therapeutic System
Decision Date1996-06-03
Product CodeIWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THE COBALT SCALPEL is the device name listed in this FDA 510(k) record. The listed applicant is Nova Therapeutic System. It received FDA 510(k) clearance on 1996-06-03 under 510(k) number K960892. The device is classified under product code IWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE COBALT SCALPEL?

THE COBALT SCALPEL is a medical device that received FDA 510(k) clearance on 1996-06-03. The listed applicant is Nova Therapeutic System. The 510(k) number is K960892.

When did THE COBALT SCALPEL receive FDA 510(k) clearance?

THE COBALT SCALPEL received FDA 510(k) clearance on 1996-06-03, under 510(k) number K960892.

Who is the listed applicant for THE COBALT SCALPEL?

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

What is the FDA product code for THE COBALT SCALPEL?

The FDA product code for THE COBALT SCALPEL is IWB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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