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FDA 510(k)

TITAN RC TACK

K-Number: K994269 · 2000-01-10

ApplicantInnovasive Devices, Inc.
Decision Date2000-01-10
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITAN RC TACK is the device name listed in this FDA 510(k) record. The listed applicant is Innovasive Devices, Inc.. It received FDA 510(k) clearance on 2000-01-10 under 510(k) number K994269. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITAN RC TACK?

TITAN RC TACK is a medical device that received FDA 510(k) clearance on 2000-01-10. The listed applicant is Innovasive Devices, Inc.. The 510(k) number is K994269.

When did TITAN RC TACK receive FDA 510(k) clearance?

TITAN RC TACK received FDA 510(k) clearance on 2000-01-10, under 510(k) number K994269.

Who is the listed applicant for TITAN RC TACK?

The FDA 510(k) record lists Innovasive Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITAN RC TACK?

The FDA product code for TITAN RC TACK is MAI.

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Other records listing Innovasive Devices, Inc. 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.

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