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FDA 510(k)

Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve

K-Number: K241853 · 2024-11-07

ApplicantVarian Medical Systems, Inc.
Decision Date2024-11-07
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-11-07 under 510(k) number K241853. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K241853.

When did Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve receive FDA 510(k) clearance?

Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve received FDA 510(k) clearance on 2024-11-07, under 510(k) number K241853.

Who is the listed applicant for Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve?

The FDA 510(k) record lists Varian Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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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.

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