Screw, Cannulated,7.0x150mm, Full Thread 491-861-150

GUDID 00846468041380

7.0x150mm, Full Thread

Pioneer Surgical Technology, Inc.

Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00846468041380
• NIH Device Record Key: 880c80e3-c4c8-4699-a30a-32c9f0ffd35c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Screw, Cannulated,7.0x150mm, Full Thread
• Version Model Number: 419-861-150
• Catalog Number: 491-861-150
• Company DUNS: 793384496
• Company Name: Pioneer Surgical Technology, Inc.
• 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: false
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00846468041380 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102903

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

[00846468041380]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-12-10

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