T2 1806-3100

GUDID 04546540654939

Target Device Recon

Stryker Trauma SA

Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm Orthopaedic implant aiming arm

• Primary Device ID: 04546540654939
• NIH Device Record Key: 6d7dc42d-2d4f-41a8-9486-4777ec979742
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: T2
• Version Model Number: 1806-3100
• Catalog Number: 1806-3100
• Company DUNS: 481999654
• Company Name: Stryker Trauma SA
• 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: true
• 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	04546540654939 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102992

FDA Product Code

• HSB: ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Sterilization

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

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

[04546540654939]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-04-12
• Device Publish Date: 2016-09-24

On-Brand Devices [T2]

• 07613327349870: Nail with Compression Screw
• 07613327349863: End Cap
• 07613327349856: Nail with Compression Screw
• 07613327349849: Nail with Compression Screw
• 07613327349832: End Cap
• 07613327349825: End Cap
• 07613327349818: Nail with Compression Screw
• 07613327349801: Nail with Compression Screw
• 07613327349795: Nail with Compression Screw
• 07613327349788: Nail with Compression Screw
• 07613327349771: Nail with Compression Screw
• 07613327349764: End Cap
• 07613327349757: End Cap
• 07613327349740: Nail with Compression Screw
• 07613327349733: Nail with Compression Screw
• 07613327349726: End Cap
• 07613327349719: Nail with Compression Screw
• 07613327349702: End Cap
• 07613327349696: Nail with Compression Screw
• 07613327349689: End Cap
• 07613327349672: End Cap
• 07613327349665: End Cap
• 07613327349658: Nail with Compression Screw
• 07613327349641: Nail with Compression Screw
• 07613327349634: End Cap
• 07613327349627: Nail with Compression Screw
• 07613327349610: Nail with Compression Screw
• 07613327349603: End Cap
• 07613327349597: End Cap
• 07613327349580: Nail with Compression Screw
• 07613327349573: Nail with Compression Screw
• 07613327349566: Nail with Compression Screw
• 07613327349559: Nail with Compression Screw
• 07613327349542: Nail with Compression Screw
• 04546540654939: Target Device Recon
• 07613327510171: 2351-0335S
• 07613327503876: 2339-0922S
• 07613327503869: 2339-1222S
• 07613327503852: 2339-1422S
• 07613327503845: 2339-1022S
• 07613327503838: 2339-1122S
• 07613327503821: 2339-1322S
• 07613327479782: Femur Retrograde Indication Tray
• 07613327479775: Femur Retrograde Insert
• 07613327479768: Femur Retrograde Proximal Targeting Tray
• 07613327423976: 2351-0330
• 07613327423969: 2351-0335
• 07613327411843: 2353-3907
• 07613327411805: 2353-3906
• 07613327411782: 2353-3908