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FDA 510(k)

CAUSSE TEF-PISTON

K-Number: K823439 · 1982-12-03

ApplicantTreace Medical, Inc.
Decision Date1982-12-03
Product CodeETB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CAUSSE TEF-PISTON is the device name listed in this FDA 510(k) record. The listed applicant is Treace Medical, Inc.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823439. The device is classified under product code ETB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAUSSE TEF-PISTON?

CAUSSE TEF-PISTON is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Treace Medical, Inc.. The 510(k) number is K823439.

When did CAUSSE TEF-PISTON receive FDA 510(k) clearance?

CAUSSE TEF-PISTON received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823439.

Who is the listed applicant for CAUSSE TEF-PISTON?

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

What is the FDA product code for CAUSSE TEF-PISTON?

The FDA product code for CAUSSE TEF-PISTON is ETB.

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Other records listing Treace Medical, Inc. as applicant

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Related Devices (Code: ETB)

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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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