AUSTIN MODIFIED PARTIAL OSSICULAR RE-
K-Number: K823918 · 1983-06-24
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Device Summary
Frequently Asked Questions
What is the AUSTIN MODIFIED PARTIAL OSSICULAR RE-?
AUSTIN MODIFIED PARTIAL OSSICULAR RE- is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Treace Medical, Inc.. The 510(k) number is K823918.
When did AUSTIN MODIFIED PARTIAL OSSICULAR RE- receive FDA 510(k) clearance?
AUSTIN MODIFIED PARTIAL OSSICULAR RE- received FDA 510(k) clearance on 1983-06-24, under 510(k) number K823918.
Who is the listed applicant for AUSTIN MODIFIED PARTIAL OSSICULAR RE-?
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 AUSTIN MODIFIED PARTIAL OSSICULAR RE-?
The FDA product code for AUSTIN MODIFIED PARTIAL OSSICULAR RE- is ETA.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Treace Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ETA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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