Cleared Traditional

K213759 - XACT Robotic System

K213759 is an FDA 510(k) clearance for XACT Robotic System, manufactured by Xact Robotics, Ltd.. The device is a Class 2 Radiology device with product code JAK cleared through the Traditional 510(k) pathway after a 297-day FDA review.

K213759 · Xact Robotics, Ltd. · Radiology device
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Sep 2022
Decision
297d
Days
Class 2
Risk

K213759 is an FDA 510(k) clearance for the XACT Robotic System, ACE Model. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Xact Robotics, Ltd. (Caesarea, IL). The FDA issued a Cleared decision on September 23, 2022 after a review of 297 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1750 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Xact Robotics, Ltd. devices

FDA 510(k) Submission Details - K213759

510(k) Number K213759 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 30, 2021
Decision Date September 23, 2022
Days to Decision 297 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
190d slower than avg
Panel avg: 107d · This submission: 297d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JAK Device Classification - Class 2, Special Controls

Product Code JAK System, X-ray, Tomography, Computed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1750
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Consultant

Hogan Lovells US LLP
Jonathan S Kahan

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

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All 635
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