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FDA 510(k)

TI-6AL-7NB URTN

K-Number: K932330 · 1996-03-08

ApplicantSynthes (Usa)
Decision Date1996-03-08
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TI-6AL-7NB URTN is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 1996-03-08 under 510(k) number K932330. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TI-6AL-7NB URTN?

TI-6AL-7NB URTN is a medical device that received FDA 510(k) clearance on 1996-03-08. The listed applicant is Synthes (Usa). The 510(k) number is K932330.

When did TI-6AL-7NB URTN receive FDA 510(k) clearance?

TI-6AL-7NB URTN received FDA 510(k) clearance on 1996-03-08, under 510(k) number K932330.

Who is the listed applicant for TI-6AL-7NB URTN?

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

What is the FDA product code for TI-6AL-7NB URTN?

The FDA product code for TI-6AL-7NB URTN is HSB.

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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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