5MS P06 S0031

GUDID 00810021861876

5MS T15 Driver, Cannulated, Sterile, Single-Use

In2Bones USA, LLC

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 00810021861876
• NIH Device Record Key: 6410055f-dfa6-4435-89c1-d7d43a71fd85
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 5MS
• Version Model Number: P06 S0031
• Catalog Number: P06 S0031
• Company DUNS: 079700711
• Company Name: In2Bones USA, LLC
• 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: 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(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810021861876 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170518

FDA Product Code

• HWR: DRIVER, PROSTHESIS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-08-04
• Device Publish Date: 2024-12-10

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• 00817906028263: 5MS, LATERAL NECK PLATE, 6H, L, TRIAL
• 00817906028256: 5MS, LATERAL NECK PLATE, 8H, L, TRIAL
• 00817906028249: 5MS, LATERAL NECK PLATE, 6H, R, TRIAL
• 00817906028232: 5MS, LATERAL NECK PLATE, 8H, R, TRIAL
• 00817906028225: 5MS, PLANTAR PLATE, TRIAL, 4H
• 00817906028218: 5MS, PLANTAR PLATE, TRIAL, 5H
• 00817906028201: COMPRESSION DRILL GUIDE, Ø2.0 & Ø2.5, ASSY
• 00817906028195: COMPRESSION DRILL GUIDE, Ø1.6 & Ø1.9, ASSY
• 00817906028188: 5MS, PSEUDO JONES PLATE TAMP
• 00817906028171: 5MS, LOCKING DRILL GUIDE, Ø1.9
• 00817906028164: 5MS, LOCKING DRILL GUIDE, Ø1.6
• 00817906028157: 5MS, JONES SCREW SIZER
• 00810021869421: 5MS, REDUCTION FORCEPS, NON-STERILE
• 00810021866123: 5MS, PLATE BENDING IRON, NON-STERILE
• 00810021864365: 5MS, PSEUDO JONES PLATE, LONG TRIAL, NON-STERILE
• 00810021864037: 5MS, PSEUDO JONES PLATE, Long
• 00810021866932: 5MS Reusable Instrument Set, NS
• 00810021861883: 5MS T25 Driver, Cannulated, Sterile, Single-Use
• 00810021861876: 5MS T15 Driver, Cannulated, Sterile, Single-Use
• 00810021861869: 5MS, T7 Driver, Solid, AO, Sterile, Single-Use