187-03-08

GUDID 10885862039118

ACETABULAR AUGMENT RASP, GROUP 3, SMALL, 8mm

Exactech, Inc.

Bone file/rasp, manual, reusable

• Primary Device ID: 10885862039118
• NIH Device Record Key: 8c1cea35-3c44-4ff8-b687-9ae7c18e57dd
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 187-03-08
• Catalog Number: 187-03-08
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Depth: 8 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885862039118 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101761

FDA Product Code

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

Sterilization

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

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

[10885862039118]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-27
• Device Publish Date: 2022-09-19

Devices Manufactured by Exactech, Inc.

• 10885862653260 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 1
• 10885862653277 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 2
• 10885862653284 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 3
• 10885862653291 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 4
• 10885862653307 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 5
• 10885862653321 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 1.5
• 10885862653338 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 2.5
• 10885862653345 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 3.5