151-10-27

GUDID 10885862029843

REAMER, STRAIGHT, 21.5mm

Exactech, Inc.

Medullary canal orthopaedic reamer, rigid

• Primary Device ID: 10885862029843
• NIH Device Record Key: f540bc76-e923-49ce-9714-4a43d44f5360
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 151-10-27
• Catalog Number: 151-10-27
• Company DUNS: 157565946
• Company Name: Exactech, 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: false
• 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 Dimensions

• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 21.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885862029843 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K010120

FDA Product Code

• LPH: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Sterilization

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

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

[10885862029843]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-02
• Device Publish Date: 2022-08-25

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• 10885862653307 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 5