Aero-AL 48922692

GUDID 07613327065473

Lumbar Cage System

Stryker Corporation

Polymeric spinal fusion cage, sterile Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage

• Primary Device ID: 07613327065473
• NIH Device Record Key: 0f71f130-9de0-4e69-a27d-1a464a982d6c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aero-AL
• Version Model Number: 48922692
• Catalog Number: 48922692
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter
• Width: 32 Millimeter
• Angle: 12 degree
• Depth: 26 Millimeter
• Height: 19 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327065473 [Primary]

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-09-24

On-Brand Devices [Aero-AL]

• 07613327067712: Lumbar Cage System
• 07613327067705: Lumbar Cage System
• 07613327067699: Lumbar Cage System
• 07613327067682: Lumbar Cage System
• 07613327067675: Lumbar Cage System
• 07613327067668: Lumbar Cage System
• 07613327067651: Lumbar Cage System
• 07613327067644: Lumbar Cage System
• 07613327067637: Lumbar Cage System
• 07613327067620: Lumbar Cage System
• 07613327067613: Lumbar Cage System
• 07613327065770: Lumbar Cage System
• 07613327065664: Fixation Anchor, White Cartridge
• 07613327065633: Fixation Anchor, Blue Cartridge
• 07613327065626: Fixation Anchor, Blue Cartridge
• 07613327065619: Fixation Anchor, White Cartridge
• 07613327065602: Lumbar Cage System
• 07613327065596: Fixation Anchor, White Cartridge
• 07613327065589: Lumbar Cage System
• 07613327065572: Fixation Anchor, Blue Cartridge
• 07613327065565: Lumbar Cage System
• 07613327065558: Lumbar Cage System
• 07613327065541: Lumbar Cage System
• 07613327065534: Lumbar Cage System
• 07613327065527: Lumbar Cage System
• 07613327065510: Lumbar Cage System
• 07613327065503: Lumbar Cage System
• 07613327065497: Lumbar Cage System
• 07613327065473: Lumbar Cage System
• 07613327065466: Lumbar Cage System
• 07613327065459: Lumbar Cage System
• 07613327065442: Lumbar Cage System
• 07613252663287: REVISION ADAPTER
• 07613252663270: REVISION ADAPTER
• 07613252663263: REVISION ADAPTER
• 07613252663256: 11 / 13 mm REVISION ADAPTER
• 07613252663072: INSERTER GUIDE
• 07613252663065: INSERTER GUIDE
• 07613252663058: INSERTER GUIDE
• 07613252663041: INSERTER GUIDE
• 07613252663034: INSERTER GUIDE
• 07613252662952: PILOT CUTTER
• 07613327273489: SOFT TISSUE GUARD
• 07613327273557: ANCHOR TAMP
• 07613327273465: MALLET
• 07613327273427: FREEHAND TAMP
• 07613327273830: TRIAL
• 07613327273786: TRIAL
• 07613327273762: TRIAL
• 07613327273755: TRIAL