Estremo Citieffe Nailing System
K-Number: K181540 · 2019-01-16
Device Summary
Frequently Asked Questions
What is the Estremo Citieffe Nailing System?
Estremo Citieffe Nailing System is a medical device that received FDA 510(k) clearance on 2019-01-16. The listed applicant is Citieffe S.R.L.. The 510(k) number is K181540.
When did Estremo Citieffe Nailing System receive FDA 510(k) clearance?
Estremo Citieffe Nailing System received FDA 510(k) clearance on 2019-01-16, under 510(k) number K181540.
Who is the listed applicant for Estremo Citieffe Nailing System?
The FDA 510(k) record lists Citieffe S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Estremo Citieffe Nailing System?
The FDA product code for Estremo Citieffe Nailing System is HSB.
Other records listing Citieffe S.R.L. 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: HSB)
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.