Who is the manufacturer of DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM?

Depuy, Inc. filed the 510(k) submission for DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM (K964024).

What is the FDA product code for DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM?

KWP. It is classified under 21 CFR 888.3050 as a Class 2 device in the Orthopedic panel.

What is the regulatory pathway for DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM?

510(k) clearance (submission type: Traditional).

What are the predicate devices for DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM?

DePuy Motech MOSS Miami Spinal System - Titanium Components (K955348); DePuy Motech MOSS Miami Spinal System (K953915).

Who can help prepare an FDA 510(k) submission like DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM

K964024 · Depuy, Inc. · KWP · Mar 26, 1997 · Orthopedic

Device Facts

Record ID	K964024
Device Name	DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM
Applicant	Depuy, Inc.
Product Code	KWP · Orthopedic
Decision Date	Mar 26, 1997
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 888.3050
Device Class	Class 2
Attributes	Therapeutic

Intended Use

The MOSS Miami Spinal System is intended for non-cervical use in the spine. When used with anterior screw fixation or posterior hook, non-pedicle screw fixation the MOSS Miami Spinal System is intended to treat scoliosis, kyphosis and lordosis, fracture, loss of stability due to tumor, spinal stenosis, spondylolisthesis, a previously failed back surgery or degenerative disc disease (i.e. discogenic back pain with degeneration of the disc confirmed by history and radiographic studies). When used with pedicle screw fixation, the MOSS Miami Spinal System is intended for use in patients with severe spondylolisthesis (Grades 3 and 4) at the L5-S1 vertebral joint, having fusions with autogenous bone graft, with the device fixed or attached to the lumbar and sacral spine (levels of pedicle screw attachment are L3 and below), and for whom the device system is intended to be removed after the development of a solid fusion mass.

Device Story

Spinal instrumentation system consisting of rods, monoaxial/polyaxial screws, hooks, and connectors; used for non-cervical spinal stabilization and fusion. System components available in stainless steel or titanium. Device implanted by surgeons during spinal procedures to provide mechanical stability while bone graft achieves fusion. Titanium screws (5mm and 8mm) added to existing system; intended for use with previously cleared MOSS Miami components. Provides structural support to spinal column; facilitates fusion in patients with degenerative or traumatic spinal conditions.

Clinical Evidence

No clinical data provided; substantial equivalence based on design and material comparison to predicate devices.

Technological Characteristics

Spinal fixation system components including longitudinal rods, monoaxial/polyaxial screws, hooks, transverse/axial connectors, and washers. Materials: Stainless steel or titanium. Dimensions: 4-5mm rods (SS), 5.5mm rods (Ti); 5-8mm screw diameters. Mechanical fixation principle. Sterilization not specified.

Indications for Use

Indicated for patients requiring non-cervical spinal fixation for scoliosis, kyphosis, lordosis, fracture, tumor-related instability, spinal stenosis, spondylolisthesis, failed back surgery, or degenerative disc disease. Pedicle screw fixation is indicated specifically for severe spondylolisthesis (Grades 3-4) at L5-S1, requiring autogenous bone graft and subsequent device removal after fusion.

Regulatory Classification

Identification

A spinal interlaminal fixation orthosis is a device intended to be implanted made of an alloy, such as stainless steel, that consists of various hooks and a posteriorly placed compression or distraction rod. The device is implanted, usually across three adjacent vertebrae, to straighten and immobilize the spine to allow bone grafts to unite and fuse the vertebrae together. The device is used primarily in the treatment of scoliosis (a lateral curvature of the spine), but it also may be used in the treatment of fracture or dislocation of the spine, grades 3 and 4 of spondylolisthesis (a dislocation of the spinal column), and lower back syndrome.

Predicate Devices

DePuy Motech MOSS Miami Spinal System - Titanium Components (K955348)
DePuy Motech MOSS Miami Spinal System (K953915)

Related Devices

K030383 — MODIFICATION TO MOSS MIAMI SPINAL SYSTEM POLYAXIAL SCREWS · Depuyacromed · Feb 26, 2003
K982511 — DEPUY MOTECH MOSS MIAMI SPINAL SYSTEMS · Depuy, Inc. · Sep 14, 1998
K972568 — DEPUY MOTECH MOSS-MIAMI SPINAL SYSTEM · Depuy, Inc. · Sep 19, 1997
K022623 — 5.0 MM DIAMETER POLYAXIAL SCREWS (MOSS MIAMI 6.35MM SYSTEM) · Depuyacromed · Aug 27, 2002
K041460 — CD HORIZON SPINAL SYSTEM · Medtronic Sofamor Danek USA, Inc. · Jul 1, 2004

Submission Summary (Full Text)

{0} K96 4024 510(k) SUMMARY MAR 26 1997 NAME OF FIRM: DePuy Inc. 700 Orthopaedic Drive Warsaw, Indiana 46581-0988 510(K) CONTACT: Cheryl Hastings Manager, Clinical Affairs TRADE NAME: DePuy Motech MOSS Miami Spinal System COMMON NAME: Rod and screw spinal instrumentation CLASSIFICATION: 888.3050 Spinal interlaminal fixation orthosis DEVICE PRODUCT CODE: 87 KWP, KWQ and MNH SUBSTANTIALLY - DePuy Motech MOSS Miami Spinal System - Titanium Components EQUIVALENT DEVICES: - DePuy Motech MOSS Miami Spinal System - Anterior Use ## INTENDED USE AND DEVICE DESCRIPTION: The MOSS Miami Spinal System is intended for non-cervical use in the spine. When used with anterior screw fixation or posterior hook, non-pedicle screw fixation the MOSS Miami Spinal System is intended to treat scoliosis, kyphosis and lordosis, fracture, loss of stability due to tumor, spinal stenosis, spondylolisthesis, a previously failed back surgery or degenerative disc disease (i.e. discogenic back pain with degeneration of the disc confirmed by history and radiographic studies). When used with pedicle screw fixation, the MOSS Miami Spinal System is intended for use in patients with severe spondylolisthesis (Grades 3 and 4) at the L5-S1 vertebral joint, having fusions with autogenous bone graft, with the device fixed or attached to the lumbar and sacral spine (levels of pedicle screw attachment are L3 and below), and for whom the device system is intended to be removed after the development of a solid fusion mass. The MOSS MIAMI System is available in either Stainless Steel or Titanium. The following components are available in Stainless Steel: 4mm and 5mm diameter longitudinal rods, 5-7mm diameter monoaxial screws, 5-7mm diameter polyaxial screws, hooks, transverse connectors, axial connectors and staple washers. The following components are available in Titanium: 5.5mm diameter longitudinal rods, 5-8mm diameter monoaxial screws, 5-7mm diameter polyaxial screws, hooks, transverse connectors, axial connectors, washers and staple washers. Titanium components of the MOSS Miami Spinal System were cleared in K955348 for the intended uses listed above. The components that were cleared included 5.5mm longitudinal smooth rods, 6 and 7mm diameter mono- and polyaxial screws, inner screws, outer locking nuts, washers, staple washers, hooks, transverse connectors and axial connectors. Additional screws with diameters of 5mm and 8mm are now being added to this system. These additional components are intended to be used with the Titanium {1} MOSS Miami rods, hooks, screws, transverse and axial connectors and outer locking nut which have previously been described and cleared for marketing in K955348. ## BASIS OF SUBSTANTIAL EQUIVALENCE: The 5 and 8mm diameter Titanium MOSS Miami screws are substantially equivalent to the screws originally cleared in K955348 (6 and 7mm diameter) in that they are manufactured from the same material, have the same intended use and have basically the same design. The only differences between the screws previously cleared and the screws that are the subject of this submission are that the 5mm screws have slightly shorter threads than the 6mm screws (but the same minor diameter) and the 8mm screws have a slightly larger diameter than the 7mm screws. The 5mm Titanium screws have the same design as the 5mm Stainless Steel screws that were cleared in K953915.