SF Push-in Anchor
K-Number: K260294 · 2026-03-27
Device Summary
Frequently Asked Questions
What is the SF Push-in Anchor?
SF Push-in Anchor is a medical device that received FDA 510(k) clearance on 2026-03-27. The listed applicant is Surgical Fusion Technologies GmbH. The 510(k) number is K260294.
When did SF Push-in Anchor receive FDA 510(k) clearance?
SF Push-in Anchor received FDA 510(k) clearance on 2026-03-27, under 510(k) number K260294.
Who is the listed applicant for SF Push-in Anchor?
The FDA 510(k) record lists Surgical Fusion Technologies GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SF Push-in Anchor?
The FDA product code for SF Push-in Anchor is MAI.
Other records listing Surgical Fusion Technologies GmbH 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: MAI)
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.