FDA 510(k)

Tryptik Ti

K-Number: K200312 · 2020-04-06

Decision Date2020-04-06

Product CodeODP

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Tryptik Ti is a medical device manufactured by Spineart. It received FDA 510(k) clearance on 2020-04-06 under approval number K200312. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tryptik Ti?

Tryptik Ti is a medical device that received FDA 510(k) clearance on 2020-04-06. It is manufactured by Spineart. The 510(k) number is K200312.

When was Tryptik Ti approved by the FDA?

Tryptik Ti received FDA 510(k) clearance on 2020-04-06, under approval number K200312.

What company makes Tryptik Ti?

Tryptik Ti is manufactured by Spineart.

What is the FDA product code for Tryptik Ti?

The FDA product code for Tryptik Ti is ODP.

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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.