Fine Osteotomy disposable instruments - Distal femur 015-330-602

GUDID 00688346000528

Distal femur, disposable instruments (cutting guides, screws, drilling tower, validators)

Laboratoires Bodycad Inc

Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide

• Primary Device ID: 00688346000528
• NIH Device Record Key: 731cdbc6-d293-4198-8405-fb1fd92b783c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fine Osteotomy disposable instruments - Distal femur
• Version Model Number: 015-330-602
• Catalog Number: 015-330-602
• Company DUNS: 202981171
• Company Name: Laboratoires Bodycad 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: false
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00688346000528 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193614

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

[00688346000528]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-12-04
• Device Publish Date: 2020-05-20

On-Brand Devices [Fine Osteotomy disposable instruments - Distal femur]

• 00688346000535: Distal femur, disposable instruments (cutting guides, screws, drilling tower)
• 00688346000528: Distal femur, disposable instruments (cutting guides, screws, drilling tower, validators)
• 00688346000115: Distal femur, disposable instruments (cutting guides, screws, drilling tower, pre-drill guide, v
• 00688346002249: cutting guides, drilling tower and retaining screws,
• 00688346002232: cutting guides, drilling tower, open validators and retaining screws
• 00688346002225: Cutting guides, drilling towers, pre-drill guide, open validators and retaining screws.