FLOWERS DORSAL COLUMELLA IMPLANT
K-Number: K904657 · 1990-12-18
Advertisement
Device Summary
Frequently Asked Questions
What is the FLOWERS DORSAL COLUMELLA IMPLANT?
FLOWERS DORSAL COLUMELLA IMPLANT is a medical device that received FDA 510(k) clearance on 1990-12-18. The listed applicant is Implantech Associates, Inc.. The 510(k) number is K904657.
When did FLOWERS DORSAL COLUMELLA IMPLANT receive FDA 510(k) clearance?
FLOWERS DORSAL COLUMELLA IMPLANT received FDA 510(k) clearance on 1990-12-18, under 510(k) number K904657.
Who is the listed applicant for FLOWERS DORSAL COLUMELLA IMPLANT?
The FDA 510(k) record lists Implantech Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLOWERS DORSAL COLUMELLA IMPLANT?
The FDA product code for FLOWERS DORSAL COLUMELLA IMPLANT is FZE.
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 Implantech Associates, 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: FZE)
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