APEX 124603000

GUDID 10603295019688

APEX HOLE ELIMINATOR - PS

DEPUY ORTHOPAEDICS, INC.

Acetabulum prosthesis hole plug

• Primary Device ID: 10603295019688
• NIH Device Record Key: c01d238a-9e85-4411-a83e-3487a2bc1a17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: APEX
• Version Model Number: 1246-03-000
• Catalog Number: 124603000
• Company DUNS: 080506581
• Company Name: DEPUY ORTHOPAEDICS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

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
• 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
• 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	10603295019688 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K963309

FDA Product Code

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

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-09-30
• Device Publish Date: 2015-09-24

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

• 10603295553519 - INHANCE: 2025-10-07 INHANCE MAKE TO ORDER PIN DRILL GUIDE - SMALL
• 10603295553526 - INHANCE: 2025-10-07 INHANCE MAKE TO ORDER PIN DRILL GUIDE - LARGE
• 10603295552628 - ATTUNE: 2025-08-05 ATTUNE MAKE TO ORDER POSTERIOR SAW CAPTURE SHIM 1.0 mm
• 10603295552635 - ATTUNE: 2025-08-05 ATTUNE MAKE TO ORDER POSTERIOR SAW CAPTURE ASSEMBLY 6 - 8
• 10603295552703 - ATTUNE: 2025-08-05 ATTUNE MAKE TO ORDER POSTERIOR SAW CAPTURE ASSEMBLY 3 - 5
• 10603295552789 - ATTUNE: 2025-08-05 ATTUNE MAKE TO ORDER POSTERIOR SAW CAPTURE SHIM 2.0 mm
• 10603295552840 - ATTUNE: 2025-08-05 ATTUNE MAKE TO ORDER POSTERIOR SAW CAPTURE SHIM 3.0 mm
• 10603295552857 - RECLAIM: 2025-08-05 RECLAIM TM MAKE TO ORDER NECK TRIAL SO