229990025

GUDID 10603295115281

CAS STRAIGHT CUP INSERTER

DEPUY ORTHOPAEDICS, INC.

Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 10603295115281
• NIH Device Record Key: 699830a7-3040-41ac-be6a-882a25ab0eb9
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 2299-90-025
• Catalog Number: 229990025
• Company DUNS: 080506581
• Company Name: DEPUY ORTHOPAEDICS, 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

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10603295115281 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071135

FDA Product Code

• HAW: Neurological stereotaxic Instrument
• HXO: PUSHER, SOCKET

Sterilization

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

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

[10603295115281]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-04-23
• Device Publish Date: 2016-06-30

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

• 10603295094081 - NA: 2025-01-10 M.B.T. EVALUATION BULLET W/PEGS SIZE 1-3
• 10603295094098 - NA: 2025-01-10 M.B.T. EVALUATION BULLET W/PEGS SIZE 4-7
• 10603295094111 - NA: 2025-01-10 M.B.T. EVALUATION BULLET W/O PEGS SIZE 1-3
• 10603295094128 - NA: 2025-01-10 M.B.T. EVALUATION BULLET W/O PEGS SIZE 4-7
• 10603295215738 - P.F.C.: 2025-01-10 P.F.C. MODULAR PLUS HEMI WEDGE TRIAL SZ 2 10 DEG
• 10603295215745 - P.F.C.: 2025-01-10 P.F.C. MODULAR PLUS HEMI WEDGE TRIAL SZ 2 20 DEG
• 10603295215776 - P.F.C.: 2025-01-10 P.F.C. MODULAR PLUS FULL WEDGE TRIAL SZ 2 10 DEG
• 10603295215783 - P.F.C.: 2025-01-10 P.F.C. MODULAR PLUS FULL WEDGE TRIAL SZ 2 15 DEG