Cleared Special

K062767 - CTL-63 AND CTL-128 SPINE ARRAY COILS

K062767 is an FDA 510(k) clearance for CTL-63 AND CTL-128 SPINE ARRAY COILS, manufactured by Invivo Corporation. The device is a Class 2 Radiology device with product code MOS cleared through the Special 510(k) pathway after a 28-day FDA review.

K062767 · Invivo Corporation · Radiology device
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Oct 2006
Decision
28d
Days
Class 2
Risk

K062767 is an FDA 510(k) clearance for the CTL-63 AND CTL-128 SPINE ARRAY COILS. Classified as Coil, Magnetic Resonance, Specialty (product code MOS), Class II - Special Controls.

Submitted by Invivo Corporation (Pewaukee, US). The FDA issued a Cleared decision on October 13, 2006 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1000 - the FDA radiology and imaging software oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Invivo Corporation devices

FDA 510(k) Submission Details - K062767

510(k) Number K062767 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 15, 2006
Decision Date October 13, 2006
Days to Decision 28 days
Submission Type Special
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 107d · This submission: 28d
Pathway characteristics
Modification to existing cleared device.

MOS Device Classification - Class 2, Special Controls

Product Code MOS Coil, Magnetic Resonance, Specialty
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1000
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 Peers - MOS Coil, Magnetic Resonance, Specialty

All 311
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