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FDA 510(k)

Tecomet Global Unite Short Stem Instrumentation

K-Number: K211553 · 2021-08-04

ApplicantSymmetry Medical Manufacturing Inc. Dba Tecomet, Inc.
Decision Date2021-08-04
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Tecomet Global Unite Short Stem Instrumentation is a medical device manufactured by Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc.. It received FDA 510(k) clearance on 2021-08-04 under approval number K211553. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tecomet Global Unite Short Stem Instrumentation?

Tecomet Global Unite Short Stem Instrumentation is a medical device that received FDA 510(k) clearance on 2021-08-04. It is manufactured by Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc.. The 510(k) number is K211553.

When was Tecomet Global Unite Short Stem Instrumentation approved by the FDA?

Tecomet Global Unite Short Stem Instrumentation received FDA 510(k) clearance on 2021-08-04, under approval number K211553.

What company makes Tecomet Global Unite Short Stem Instrumentation?

Tecomet Global Unite Short Stem Instrumentation is manufactured by Symmetry Medical Manufacturing Inc. Dba Tecomet, Inc..

What is the FDA product code for Tecomet Global Unite Short Stem Instrumentation?

The FDA product code for Tecomet Global Unite Short Stem Instrumentation is PHX.

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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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