RICHARDS TOTAL/PARTIAL PROSTHESIS
K-Number: K962564 · 1997-01-22
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Device Summary
Frequently Asked Questions
What is the RICHARDS TOTAL/PARTIAL PROSTHESIS?
RICHARDS TOTAL/PARTIAL PROSTHESIS is a medical device that received FDA 510(k) clearance on 1997-01-22. The listed applicant is Gyrus Ent LLC. The 510(k) number is K962564.
When did RICHARDS TOTAL/PARTIAL PROSTHESIS receive FDA 510(k) clearance?
RICHARDS TOTAL/PARTIAL PROSTHESIS received FDA 510(k) clearance on 1997-01-22, under 510(k) number K962564.
Who is the listed applicant for RICHARDS TOTAL/PARTIAL PROSTHESIS?
The FDA 510(k) record lists Gyrus Ent LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RICHARDS TOTAL/PARTIAL PROSTHESIS?
The FDA product code for RICHARDS TOTAL/PARTIAL PROSTHESIS is ETB.
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 Gyrus Ent LLC 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: ETB)
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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