MEDRAD PHASED ARRAY 1.5T SHOULDER IMAGING SURFACE COIL
Device Facts
| Record ID | K960901 |
|---|---|
| Device Name | MEDRAD PHASED ARRAY 1.5T SHOULDER IMAGING SURFACE COIL |
| Applicant | Medrad, Inc. |
| Product Code | LNH · Radiology |
| Decision Date | May 29, 1996 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 892.1000 |
| Device Class | Class 2 |
Indications for Use
The Medrad Phased Array 1.5T Shoulder Imaging Surface Coil is for use only with the GEMS family of Super Conductor MR Systems. An anterior loop pair is combined with a posterior loop. The coil is designed to receive RF excitation from the protons of the hydrogen nuclei as a result of the scanner exciting these protons. The coil is designed for anatomical imaging of either the right or left shoulder region with a specific size and shape to facilitate placement on the anatomy area of interest. This placement results in a higher Signal To Noise Ratio(SNR) in the region near the surface coil. The greater SNR permits more effective imaging through the use of a smaller FOV and thinner slices. The intended ROI for imaging includes the anterior and posterior musculoskeletal area of the shoulder. This includes the rotator cuff, humeral head, glenoid, glenoid labrum and glenoid cavity. The region runs superior through the clavicle and acromion and inferior through the infraspinatus. It also extends posterior to the lateral margin. The Medrad Phased Array 1.5T Shoulder Imaging Surface Coil is intended for use in physician diagnosis of impingement syndrome, glenoid labrum tendon tears, rotator cuff tears, edema secondary to the aforementioned, retraction of the supraspinatus muscle and trauma of the long head of the biceps tendon. Patient fitness and suitability for MRI must be determined by the individual physician trained in the field of Diagnostic Magnetic Resonance Imaging.
Device Story
Rigid RF receive-only magnetic field pickup coil; designed for 1.5T MRI shoulder imaging. Input: RF excitation from hydrogen nuclei protons. Operation: Phased array technology; anterior/posterior loop configuration; interfaces with GEMS Signa System multi-coil port. Output: High-resolution MR images. Used in clinical settings by trained MRI physicians. Output allows visualization of musculoskeletal structures (rotator cuff, labrum, etc.) to aid diagnosis of tears, impingement, and trauma. Benefits: Higher Signal-to-Noise Ratio (SNR) compared to linear coils; enables smaller field of view and thinner slices for improved diagnostic detail.
Clinical Evidence
Bench testing performed per NEMA Standard No. 6 to characterize SNR and image non-uniformity using loaded phantoms. Safety testing included temperature rise and IEC 601-1 dielectric strength testing. Clinical evidence consisted of comparative imaging between the subject device and the predicate Linear 1.5T Shoulder Coil, demonstrating improved SNR and morphological detail.
Technological Characteristics
Receive-only dual-loop phased array coil; ABS outer housing; Velcro/latch fasteners. Compatible with GEMS 1.5T Signa systems via quick-disconnect port. No external tuning/matching required. Designed to limit surface temperature to <41°C. Non-ferrous construction.
Indications for Use
Indicated for patients requiring MRI imaging of the shoulder region (rotator cuff, humeral head, glenoid, glenoid labrum, glenoid cavity, clavicle, acromion, infraspinatus) for diagnosis of impingement syndrome, tendon tears, edema, muscle retraction, or trauma.
Regulatory Classification
Identification
A magnetic resonance diagnostic device is intended for general diagnostic use to present images which reflect the spatial distribution and/or magnetic resonance spectra which reflect frequency and distribution of nuclei exhibiting nuclear magnetic resonance. Other physical parameters derived from the images and/or spectra may also be produced. The device includes hydrogen-1 (proton) imaging, sodium-23 imaging, hydrogen-1 spectroscopy, phosphorus-31 spectroscopy, and chemical shift imaging (preserving simultaneous frequency and spatial information).
Special Controls
*Classification.* Class II (special controls). A magnetic resonance imaging disposable kit intended for use with a magnetic resonance diagnostic device only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.