LITe Plate System 49175544

GUDID 07613327066593

REVISION SCREW

Stryker Corporation

Spinal fixation plate, non-bioabsorbable

• Primary Device ID: 07613327066593
• NIH Device Record Key: 18dadcaa-d58e-490d-bf10-f6a951574b65
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LITe Plate System
• Version Model Number: 49175544
• Catalog Number: 49175544
• 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: false
• 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

• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0
• Length: 44 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327066593 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142699

FDA Product Code

• KWQ: APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

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

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

[07613327066593]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-09-14

On-Brand Devices [LITe Plate System]

• 07613327068115: STANDARD SCREW
• 07613327068108: STANDARD SCREW
• 07613327068092: STANDARD SCREW
• 07613327068085: STANDARD SCREW
• 07613327068078: STANDARD SCREW
• 07613327068047: 1 LEVEL 4-SCREW PLATE
• 07613327068023: 1 LEVEL 4-SCREW PLATE
• 07613327068016: 1 LEVEL 4-SCREW PLATE
• 07613327068009: 1 LEVEL 4-SCREW PLATE
• 07613327067996: 1 LEVEL 4-SCREW PLATE
• 07613327067989: 1 LEVEL 4-SCREW PLATE
• 07613327067972: 1 LEVEL 2-SCREW PLATE
• 07613327067965: 1 LEVEL 2-SCREW PLATE
• 07613327067958: 1 LEVEL 2-SCREW PLATE
• 07613327067941: 1 LEVEL 2-SCREW PLATE
• 07613327067934: 1 LEVEL 2-SCREW PLATE
• 07613327067927: 1 LEVEL 2-SCREW PLATE
• 07613327066630: REVISION SCREW
• 07613327066623: REVISION SCREW
• 07613327066616: REVISION SCREW
• 07613327066609: REVISION SCREW
• 07613327066593: REVISION SCREW
• 07613327066586: REVISION SCREW
• 07613327066579: REVISION SCREW
• 07613327066562: REVISION SCREW
• 07613327066555: REVISION SCREW
• 07613327066548: REVISION SCREW
• 07613327066531: REVISION SCREW
• 07613327066524: REVISION SCREW
• 07613327066517: STANDARD SCREW
• 07613327066500: STANDARD SCREW
• 07613327066494: STANDARD SCREW
• 07613327066487: STANDARD SCREW
• 07613327066470: STANDARD SCREW
• 07613327066463: STANDARD SCREW
• 07613327066456: STANDARD SCREW
• 07613327066449: 1 LEVEL 2-SCREW PLATE
• 07613327066432: 1 LEVEL SACRAL PLATE
• 07613327066425: 1 LEVEL SACRAL PLATE
• 07613327066418: BUTTRESS PLATE
• 07613327066401: 1 LEVEL SACRAL PLATE
• 07613327066395: 1 LEVEL SACRAL PLATE
• 07613327066388: 1 LEVEL SACRAL PLATE
• 07613327066371: 1 LEVEL SACRAL PLATE
• 07613327066364: 1 LEVEL SACRAL PLATE
• 07613327066357: 1 LEVEL SACRAL PLATE
• 07613327066340: 1 LEVEL UNIVERSAL PLATE
• 07613327066333: 1 LEVEL UNIVERSAL PLATE
• 07613327066326: 1 LEVEL SACRAL PLATE
• 07613327066319: 1 LEVEL UNIVERSAL PLATE