SF Push- in Anchor
K-Number: K240288 · 2024-04-01
ApplicantSurgical Fusion Technologies GmbH
Decision Date2024-04-01
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
SF Push- in Anchor is a medical device manufactured by Surgical Fusion Technologies GmbH. It received FDA 510(k) clearance on 2024-04-01 under approval number K240288. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
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 2024-04-01. It is manufactured by Surgical Fusion Technologies GmbH. The 510(k) number is K240288.
When was SF Push- in Anchor approved by the FDA?
SF Push- in Anchor received FDA 510(k) clearance on 2024-04-01, under approval number K240288.
What company makes SF Push- in Anchor?
SF Push- in Anchor is manufactured by Surgical Fusion Technologies GmbH.
What is the FDA product code for SF Push- in Anchor?
The FDA product code for SF Push- in Anchor is MAI.
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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.