0306620000

GUDID 07613252574187

Curette

STRYKER CORPORATION

Spinal curette

• Primary Device ID: 07613252574187
• NIH Device Record Key: bfd93e61-061c-4ca6-9300-73b2cf48679a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0306620000
• Catalog Number: 0306620000
• 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: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge
• Needle Gauge: 10 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613252574187 [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

Devices Manufactured by STRYKER CORPORATION

• 07613327628357 - RPS: 2026-03-19 SAW ONE
• 07613327656763 - BPX: 2026-03-12 Pistol Battery
• 07613327656770 - BPX: 2026-03-12 Pencil Battery
• 07613327657760 - BPX: 2026-03-12 Sagittal Saw
• 07613327657777 - BPX: 2026-03-12 Micro Drill
• 07613327657784 - BPX: 2026-03-12 Oscillating Saw
• 07613327657791 - BPX: 2026-03-12 Universal Driver
• 07613327657807 - N/A: 2026-03-12 Handpiece Insert Tray - Top