The EXPEDIUM Spine System is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine.

The EXPEDIUM™ Spine System is intended for noncervical pedicle fixation and nonpedicle fixation for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e., fracture or dislocation); spinal stenosis; curvatures (i.e., scoliosis, kyphosis, and/or lordosis); tumor; pseudarthrosis; and failed previous fusion in skeletally mature patients.

Device Description

The subject EXPEDIUM™ Spine System components are designed to accept a 6.35mm rod and are available in various geometries and sizes. The EXPEDIUM™ Spine System also contains Class I manual surgical instruments, trays and cases and are exempt from premarket notification.

AI/ML Overview

The provided text is a 510(k) summary for a medical device called the "EXPEDIUM™ Spine System." This document is a regulatory submission to the FDA for a medical device and describes its intended use and materials. It does not contain information about acceptance criteria, device performance metrics, sample sizes, expert qualifications, or study methodologies that would be typical for proving a device meets acceptance criteria in the manner requested.

The document states:

"Performance data per ASTM F 1798 were submitted to characterize the subject EXPEDIUM™ Spine System components addressed in this notification."

This indicates that mechanical performance data according to a specific ASTM standard (F 1798) was provided to the FDA. However, the exact acceptance criteria, the specific test results, the sample sizes for these tests, or any details about clinical studies (which would involve human readers, ground truth, etc.) are not present in this 510(k) summary. These summaries typically focus on device description, intended use, and substantial equivalence to predicate devices, rather than detailed study results.

Therefore, I cannot populate the requested table and answer the questions based solely on the provided text, as the information required to do so is not present. The document focuses on regulatory compliance based on mechanical testing and comparison to predicate devices, not on a clinical performance study with human readers or image analysis.

Summary

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Special 510(k) Submission -- Additions to EXPEDIUM™ Spine System

6. 510(K) SUMMARY

Submitter:	DePuy Spine, Inc.325 Paramount DriveRaynham, MA 02767	MAY - 8 2008
Contact Person:	Christopher Klaczyk, Regulatory Project ManagerVoice: (508) 828-2852Fax: (508) 828-3797
Date Prepared:	February 5, 2008
Device Class:	Class III
Classification Name:	Spinal interlaminar fixation orthosisper 21 CFR §888.3050
	Pedicle screw spinal fixationper 21 CFR §888.3070
Classification Panel:	Orthopedics
FDA Panel Number:	87
Product Code(s):	NKB, MNH, MNI, KWP
Proprietary Name:	EXPEDIUM™ Spine System
Predicate Devices:	EXPEDIUM™ 6.35mm Spine System (K062174,K063156, K063741)
Device Description:	The subject EXPEDIUM™ Spine System components aredesigned to accept a 6.35mm rod and are available invarious geometries and sizes.
	The EXPEDIUM™ Spine System also contains Class Imanual surgical instruments, trays and cases and areexempt from premarket notification.

DePuy Spine, Inc., a Johnson & Johnson Company

Page 1 of 2

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The EXPEDIUM Spine System is intended to provide Intended Use: immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine.

The EXPEDIUM Spinc System is intended for noncervical pedicle fixation and nonpedicle fixation for the following indications: degenerative disc discase (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.c., fracture or dislocation); spinal stenosis; curvatures (i.e., scoliosis, kyphosis, and/or lordosis); tumor; pseudoarthrosis; and failed previous fusion in skeletally mature patients.

Manufactured from ASTM F 138 implant grade stainless Materials: steel and ASTM F 136 implant grade titanium alloy.
Performance data per ASTM F 1798 were submitted to Performance Data: characterize the subject EXPEDIUM™ Spine System components addressed in this notification.

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Image /page/2/Picture/1 description: The image shows the seal of the Department of Health & Human Services - USA. The seal features a stylized caduceus, a symbol often associated with medicine and healthcare, on the right side. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the caduceus. The seal is presented in black and white.

Public Health Service

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

MAY - 8 2008

DePuy Spine, Inc. % Mr. Christopher Klaczyk Regulatory Project Manager 325 Paramount Drive Raynham, MA 02767

Re: K080313

Trade/Device Name: EXPEDIUMTM Spine System Regulation Number: 21 CFR 888.3070 Regulation Name: Pedicle screw spinal system Regulatory Class: Class III Product Code: NKB, MNH, MNI, KWP Dated: April 23, 2008 Received: April 24, 2008

Dear Mr. Klaczyk:

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 (PMA), 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.

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.

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Page 2 - Mr. Christopher Klaczyk

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 (240) 276-0120. 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 toll-free number (800) 638-2041 or (240) 276-3150 or the Internet address http://www.fda.gov/cdrh/industry/support/index.html.

Sincerely yours,

Mark H. Millman

Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Special 510(k) Submission -- Additions to EXPEDIUM™ Spine System

INDICATIONS FOR USE STATEMENT 5.

( 080312 510(k) Number (if known):

Device Name: EXPEDIUM™ Spine System

Indications For Use:

Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR

Over-The-Counter Use (21 CFR 807 Subpart C)

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

Concurrence of CDRH, Office of Device Evaluation (ODE)

Neil K. Ogle for mtn

Division of General, and Neurological De

510(k) Number K080313

DePuy Spine, Inc., a Johnson & Johnson Company

Regulation Number and Section

N/A