Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve
K-Number: K241853 · 2024-11-07
Device Summary
Frequently Asked Questions
What is the Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve?
Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve is a medical device that received FDA 510(k) clearance on 2024-11-07. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K241853.
When was Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve approved by the FDA?
Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve received FDA 510(k) clearance on 2024-11-07, under approval number K241853.
What company makes Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve?
Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve is manufactured by Varian Medical Systems, Inc..
What is the FDA product code for Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve?
The FDA product code for Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve is JAQ.
Related Clinical Trials
Other Devices by Varian Medical Systems, Inc.
Related Devices (Code: JAQ)
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.