0306621000

GUDID 07613252639794

Curette

STRYKER CORPORATION

Spinal curette

• Primary Device ID: 07613252639794
• NIH Device Record Key: a11e2265-48e7-4e75-a529-042b47f0901c
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0306621000
• Catalog Number: 0306621000
• Company DUNS: 196548481
• Company Name: STRYKER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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

Customer Support Contacts

• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com

Device Dimensions

• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge
• Needle Gauge: 11 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613252639794 [Primary]

FDA Product Code

• OCJ: spinal channeling instrument, vertebroplasty

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-25
• Device Publish Date: 2018-09-24

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• 07613327006964 - ES2 SPINAL SYSTEM: 2024-09-11 ROD INSERTER
• 07613327006995 - ES2 SPINAL SYSTEM: 2024-09-11 RECOVERY GUIDE
• 07613327007008 - ES2 SPINAL SYSTEM: 2024-09-11 INNER SHAFT, RECOVERY SYSTEM
• 07613327007022 - ES2 SPINAL SYSTEM: 2024-09-11 THREADED RECOVERY GUIDE
• 07613327007046 - ES2 SPINAL SYSTEM: 2024-09-11 ROD INSERTER
• 07613327114867 - XIA 4.5 EVOLUTION: 2024-09-11 BLOCKER INSERTER
• 07613327121964 - UniVise Spinous Process Fixation Plate System: 2024-09-11 INSERTER