MRJ EXTENDED

K080098 · Paramed S.R.L. · LNH · Mar 10, 2008 · Radiology

Device Facts

• Record ID: K080098
• Device Name: MRJ EXTENDED
• Applicant: Paramed S.R.L.
• Product Code: LNH · Radiology
• Decision Date: Mar 10, 2008
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.1000
• Device Class: Class 2

Intended Use

The intended use of Paramed's MRJ_Extended product is for diagnostic nuclear magnetic resonance imaging of hip, knee, ankle, foot, shoulder, elbow, wrist, hand, call, thigh, arm, forearm, Temporo Mandibular Joint (TMJ), C- spine and L-Spine with limitation to joint pathologies (no tumors, no anglography). The device produces transverse, sagittal, coronal and oblique cross-sectional images, displaying the internal structure of the limbs and joint being imaged. The images that are produced correspond to the spatial distribution of protons (hydrogen nuclei) that check the magnetic resonance properties and depend upon the MR parameters (spin-lattice relaxation time (T1), spin-spin relaxation fime (T2), nuclei density, flow velocity and chemical shift). If interpreted by a medical expert, these images can provide diagnostically useful information.

Device Story

MRJ_Extended is a magnetic resonance imaging (MRI) system; captures proton density and relaxation properties (T1, T2) to generate cross-sectional images (transverse, sagittal, coronal, oblique). Used in clinical settings by trained professionals to visualize internal limb and joint structures. Output consists of diagnostic images for expert interpretation; aids in identifying joint pathologies. System utilizes dedicated receipt coils and extended field-of-view (FOV) for L-spine imaging. Device provides non-invasive diagnostic information to support clinical decision-making regarding musculoskeletal conditions.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

Magnetic resonance diagnostic device; utilizes dedicated receipt coils and extended FOV for L-spine imaging. Operates via nuclear magnetic resonance principles to produce cross-sectional images based on proton density and relaxation times (T1, T2).

Indications for Use

Indicated for diagnostic MRI of hip, knee, ankle, foot, shoulder, elbow, wrist, hand, calf, thigh, arm, forearm, TMJ, C-spine, and L-spine. Limited to joint pathologies; excludes tumor detection and angiography.

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.

Predicate Devices

• Paramed MrJ (K033507)
• Esaote S-Scan (K063207)

Submission Summary (Full Text)

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PARAMed

K080098

# MAR 1 0 2008

### A.3.9 510(K) Summary of Safety and Effectiveness

The following 510(k) summary has been prepared pursuant to requirements specified in 21CFR 807.92(a).

:

### Manufacturer Information

| Manufacturer: | Paramed Srl |
|------------------------------------|------------------------------------------|
| Address: | Corso Perrone 73R<br>16152 Genova, Italy |
| Establishment registration number: | To be filed |

#### 807.92(a)(1)

#### Submitter Information

| Correspondent: | Michael A. Douglas, |
|-----------------|---------------------|
| | 739 High Street |
| | North Andover, |
| | MA 01845 USA. |
| Ph: | 978.975.7530 x4345 |
| Fax: | 978.975.9930 |
| Contact person: | Michael A. Douglas |

### 807.92(a)(2)

| Trade Name: | MRJ_Extended |
|-------------------------------------|--------------------------------------------|
| Common Name: | Magnetic resonance diagnostic device |
| Classification Name(s): | System, Nuclear Magnetic Resonance Imaging |
| Classification and class of device: | 21 CFR 892.1000, class II |
| Classification Number: | 90LNH |

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一篇: 上一篇: 人

#### 807.92(a)(3)

#### Predicate Devices

Paramed MrJ K033507 for all items excluded the L-spine coils/district of examination for which the

Esaote S-Scan K063207 is addressed

#### 807.92(a)(5)

#### Device Intended Use(s)

The MrJ Extended intended use is the one of the predicate MrJ device (included the restrictions and limitations there claimed) plus the following option:

This device can produce diagnostic images of the L-Spine district using for that purpose an extended FOV and dedicated receipt coils (also the L-spine application is limited by the exclusion of tumor detection application).

#### 807.92(a)(6)

#### Technological Characteristics

The MRJ Extended MRI system is substantially equivalent to the currently available Paramed MrJ cleared via K033507 for all items excluded the spine coils for which the and Esaote S-Scan system cleared via K063207 is addressed.

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| See OMB Statement on Reverse. Form Approved: OMB No. 0910-0616, Expiration Date: 06-30-2008 | |
|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| DEPARTMENT OF HEALTH AND HUMAN SERVICES<br>Food and Drug Administration | |
| Certification of Compliance, under 42 U.S.C. § 282(j)(5)(B), with<br>Requirements of ClinicalTrials.gov Data Bank (42 U.S.C. § 282(j)) | |
| (For submission with an application/submission, including amendments, supplements, and resubmissions, under §§ 505, 515, 520(m), or 510(k) of the<br>Federal Food, Drug, and Cosmetic Act or § 351 of the Public Health Service Act.) | |
| 1. NAME OF SPONSOR/APPLICANT/SUBMITTER | PARAMED S.R.L |
| 2. DATE OF THE APPLICATION/SUBMISSION<br>WHICH THIS CERTIFICATION ACCOMPANIES | JANUARY 08 2008 |
| 3. ADDRESS (Number, Street, State, and ZIP Code) | CORSO FM PERRONE 732<br>16152 GENOA (ITALY) |
| 4. TELEPHONE AND FAX NUMBER<br>(Include Area Code) | (Tel.) [phone]<br>(Fax) " |
| PRODUCT INFORMATION | |
| 5. FOR DRUGS/BIOLOGICS: Include Any/All Available Established, Proprietary and/or Chemical/Biochemical/Blood/Cellular/Gene Therapy Product Name(s)<br>FOR DEVICES: Include Any/All Common or Usual Name(s), Classification, Trade or Proprietary or Model Name(s) and/or Model Number(s)<br>(Attach extra pages as necessary) | MODEL MRT-EXTENDED<br>CODE 01-1872-00 |
| APPLICATION / SUBMISSION INFORMATION | |
| 6. TYPE OF APPLICATION/SUBMISSION WHICH THIS CERTIFICATION ACCOMPANIES | <label><input type="checkbox"/>IND</label> <label><input type="checkbox"/>NDA</label> <label><input type="checkbox"/>ANDA</label> <label><input type="checkbox"/>BLA</label> <label><input type="checkbox"/>PMA</label> <label><input type="checkbox"/>HDE</label> <label><input checked="" type="checkbox"/>510(k)</label> <label><input type="checkbox"/>PDP</label> <label><input type="checkbox"/>Other</label> |
| 7. INCLUDE IND/NDA/ANDA/BLA/PMA/HDE/510(k)/PDP/OTHER NUMBER (If number previously assigned) | K080098 |
| 8. SERIAL NUMBER ASSIGNED TO APPLICATION/SUBMISSION WHICH THIS CERTIFICATION ACCOMPANIES | |
| CERTIFICATION STATEMENT / INFORMATION | |
| 9. CHECK ONLY ONE OF THE FOLLOWING BOXES (See instructions for additional information and explanation) | <label><input checked="" type="checkbox"/>A. I certify that the requirements of 42 U.S.C. § 282(j), Section 402(j) of the Public Health Service Act, enacted by 121 Stat. 823, Public Law<br/> 110-85, do not apply because the application/submission which this certification accompanies does not reference any clinical trial.</label><br><label><input type="checkbox"/>B. I certify that the requirements of 42 U.S.C. § 282(j), Section 402(j) of the Public Health Service Act, enacted by 121 Stat. 823, Public Law<br/> 110-85, do not apply to any clinical trial referenced in the application/submission which this certification accompanies.</label><br><label><input type="checkbox"/>C. I certify that the requirements of 42 U.S.C. § 282(j), Section 402(j) of the Public Health Service Act, enacted by 121 Stat. 823, Public Law<br/> 110-85, apply to one or more of the clinical trials referenced in the application/submission which this certification accompanies and that<br/> those requirements have been met.</label> |
| 10. IF YOU CHECKED BOX C, IN NUMBER 9, PROVIDE THE NATIONAL CLINICAL TRIAL (NCT) NUMBER(S) FOR ANY "APPLICABLE CLINICAL TRIAL(S),"<br>UNDER 42 U.S.C. § 282(j)(1)(A)(i), SECTION 402(j)(1)(A)(i) OF THE PUBLIC HEALTH SERVICE ACT, REFERENCED IN THE APPLICATION/<br>SUBMISSION WHICH THIS CERTIFICATION ACCOMPANIES (Attach extra pages as necessary) | NCT Number(s): |
| The undersigned declares, to the best of her/his knowledge, that this is an accurate, true, and complete submission of information. I understand that the<br>failure to submit the certification required by 42 U.S.C. § 282(j)(5)(B), section 402(j)(5)(B) of the Public Health Service Act, and the knowing submission<br>of a false certification under such section are prohibited acts under 21 U.S.C. § 331/section 301 of the Federal Food, Drug, and Cosmetic Act.<br>Warning: A willfully and knowingly false statement is a criminal offense, U.S. Code, title 18, section 1001. | |
| 11. SIGNATURE OF SPONSOR/APPLICANT/SUBMITTER OR AN<br>AUTHORIZED REPRESENTATIVE (Sign) | <img alt="Signature" src="signature.png"/> |
| 12. NAME AND TITLE OF THE PERON WHO SIGNED IN NO. 11 | (Name) GIAN ERICO TARDIVELLI<br>(Title) AUTHORIZED OFFICIER |
| 13. ADDRESS (Number, Street, State, and ZIP Code) (of person identified<br>in No. 11 and 12) | VIALE FRANCESCO GAMBARO 5/2<br>16146 GENOA (ITALY) |
| 14. TELEPHONE AND FAX NUMBER<br>(Include Area Code) | (Tel.) 010/7404530<br>(Fax) 010/7404530 |
| 15. DATE OF<br>CERTIFICATION | 04 FEB 2008 |
| FDA-3674 (1/08) (FRONT) | |
| PSC Graphics: [phone] EF | |

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: (301) 443-10

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: 中国 中

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Image /page/3/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized image of an eagle with its wings spread.

Food and Drug Administration 9200 Corporate Blvd. Rockville MD 20850

## MAR 1 0 2008

Paramed SRL % Mr. Michael A. Douglas Correspondent Paramed Medical Systems 739 High Street NORTH ANDOVER MA 01845

Re: K080098

Trade/Device Name: MRJ_Extended Regulation Number: 21 CFR §892.1000 Regulation Name: Magnetic resonance diagnostic device Regulatory Class: II Product Code: LNH Dated: January 8, 2008 Received: January 16, 2008

#### Dear Mr. Douglas:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Image /page/3/Picture/10 description: The image shows a circular logo for the FDA Centennial, celebrating the years 1906-2006. The logo features the letters "FDA" in a bold, stylized font at the center. Below the letters, the word "Centennial" is written in a cursive font. The logo is surrounded by a circular border with text and stars, giving it an official and commemorative appearance.

*Protecting and Promoting Public Health*

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Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally. marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Center for Devices and Radiological Health's (CDRH's) Office of Compliance at one of the following numbers, based on the regulation number at the top of this letter.

| 21 CFR 876.xxxx | (Gastroenterology/Renal/Urology) | 240-276-0115 |
|-----------------|----------------------------------|--------------|
| 21 CFR 884.xxxx | (Obstetrics/Gynecology) | 240-276-0115 |
| 21 CFR 892.xxxx | (Radiology) | 240-276-0120 |
| Other | | 240-276-0100 |

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding postmarket surveillance, please contact CDRH's Office of Surveillance and Biometric's (OSB's) Division of Postmarket Surveillance at 240-276-3474. For questions regarding the reporting of device adverse events (Medical Device Reporting (MDR)), please contact the Division of Surveillance Systems at 240-276-3464. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.

Sincerely vours.

Nancy C. Brogdon

Nancy C. Brogdon Director, Division of Reproductive. Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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#### Indications for Use

#### K080098 510(K) Number (if known):

Device Name: MRJ Extended

Indications For Use:

The intended use of Paramed's MRJ_Extended product is for diagnostic nuclear magnetic resonance imaging of hip, knee, ankle, foot, shoulder, elbow, wrist, hand, call, thigh, arm, forearm, Temporo Mandibular Joint (TMJ), C- spine and L-Spine with limitation to joint pathologies (no tumors, no anglography). The device produces transverse, sagittal, coronal and oblique cross-sectional images, displaying the internal structure of the limbs and joint being imaged. The images that are produced correspond to the spatial distribution of protons (hydrogen nuclei) that check the magnetic resonance properties and depend upon the MR parameters (spin-lattice relaxation time (T1), spin-spin relaxation fime (T2), nuclei density, flow velocity and chemical shift). If interpreted by a medical expert, these images can provide diagnostically useful information.

Prescription Use X (Part 21 CFR 801 Subpart D)

AND/OR

Over - The -Counter Use (21 CFR 801 Subpart C)

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

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Lord In Whan

(Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Device 510(k) Number