AUSTIN MODIFIED TOTAL OSSICULAR REPLACE
K-Number: K823912 · 1983-06-24
Advertisement
Device Summary
Frequently Asked Questions
What is the AUSTIN MODIFIED TOTAL OSSICULAR REPLACE?
AUSTIN MODIFIED TOTAL OSSICULAR REPLACE 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 K823912.
When did AUSTIN MODIFIED TOTAL OSSICULAR REPLACE receive FDA 510(k) clearance?
AUSTIN MODIFIED TOTAL OSSICULAR REPLACE received FDA 510(k) clearance on 1983-06-24, under 510(k) number K823912.
Who is the listed applicant for AUSTIN MODIFIED TOTAL OSSICULAR REPLACE?
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 TOTAL OSSICULAR REPLACE?
The FDA product code for AUSTIN MODIFIED TOTAL OSSICULAR REPLACE 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.
Advertisement