KOENIG TOTAL TOE IMPLANT
K-Number: K884561 · 1989-01-24
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Device Summary
Frequently Asked Questions
What is the KOENIG TOTAL TOE IMPLANT?
KOENIG TOTAL TOE IMPLANT is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is Dow Corning Wright. The 510(k) number is K884561.
When did KOENIG TOTAL TOE IMPLANT receive FDA 510(k) clearance?
KOENIG TOTAL TOE IMPLANT received FDA 510(k) clearance on 1989-01-24, under 510(k) number K884561.
Who is the listed applicant for KOENIG TOTAL TOE IMPLANT?
The FDA 510(k) record lists Dow Corning Wright as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KOENIG TOTAL TOE IMPLANT?
The FDA product code for KOENIG TOTAL TOE IMPLANT is LZJ.
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 Dow Corning Wright 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: LZJ)
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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