RevMed

NVISION BIOMEDICAL TECHNOLOGIES, INC. EARP-T-2235-0614 EARP INSTRUMENTS

Company Name
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Catalog Number
EARP-T-2235-0614
Device Size
  • Width: Millimeter
  • Depth: Millimeter
  • Height: Millimeter

Description

EARP, TRIAL 22X35X14 6° The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDD patients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.
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Summary

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Additional Details

Device Identifier
00810135960885
Is RX
No
Is Over the Counter
No
Requires Sterilization
Yes
Is Sterile
No
Is Single Use
No

Barcode Mapping

Unit of MeasurementEachesGTIN
Each100810135960885