TruAbutment DS; TruBase
K-Number: K241485 · 2024-10-09
Device Summary
Frequently Asked Questions
What is the TruAbutment DS; TruBase?
TruAbutment DS; TruBase is a medical device that received FDA 510(k) clearance on 2024-10-09. The listed applicant is Truabutment, Inc.. The 510(k) number is K241485.
When did TruAbutment DS; TruBase receive FDA 510(k) clearance?
TruAbutment DS; TruBase received FDA 510(k) clearance on 2024-10-09, under 510(k) number K241485.
Who is the listed applicant for TruAbutment DS; TruBase?
The FDA 510(k) record lists Truabutment, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TruAbutment DS; TruBase?
The FDA product code for TruAbutment DS; TruBase is NHA.
Other records listing Truabutment, 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: NHA)
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.