For Sale ARTHREX AR-9200-25 Univers VaultLock Keel Glenoid Instrument Set AR-9222 AR-9220

MPN: AR-9200-25
Arthrex Univers VaultLock Keel Glenoid Instrument Set AR-9200-25, AR-9222, AR-9220, AR-9215-3

This Arthrex Univers VaultLock Keel Glenoid Instrument Set is in great working and cosmetic condition.

What's Included:

Arthrex Trial Implant (Long); (REF - AR-9200-25); Qty: 2

Arthrex Trial Implant 6; (REF - AR-9200-16S); Qty: 1

Arthrex Trial Implant 7; (REF - AR-9200-17S); Qty: 1

Arthrex Trial Implant 8; (REF - AR-9200-18S); Qty: 1

Arthrex Trial Implant 9; (REF - AR-9200-19S); Qty: 1

Arthrex Trial Implant 10; (REF - AR-9200-20S); Qty: 1

Arthrex Trial Implant 11; (REF - AR-9200-21S); Qty: 1

Arthrex Trial Implant 12; (REF - AR-9200-22S); Qty: 1

Arthrex Trial Implant 13; (REF - AR-9200-24S); Qty: 1

Arthrex Trial Implant 14; (REF - AR-9200-25S); Qty: 1

Arthrex Trial Implant 15; (REF - AR-9200-26S); Qty: 1

Arthrex MPR Posterior Glenoid Retractor; (REF - AR-9203-25); Qty: 1

Arthrex Angled Glenrod Reamer Shaft; (REF - AR-9222); Qty: 1

Arthrex 6mm Drill; (REF - AR-9221); Qty: 1

Arthrex 6mm Drill (Long); (REF - AR-9216-1); Qty: 1

Arthrex Nautlius Glenoid Reamer (Small); (REF - AR-9220); Qty: 1

Arthrex Nautlius Glenoid Reamer (Medium); (REF - AR-9213); Qty: 1

Arthrex Nautlius Glenoid Reamer (Large); (REF - AR-9210); Qty: 1

Arthrex Nautlius Glenoid Reamer (X-Large); (REF - AR-9206); Qty: 1

Arthrex Nautlius Glenoid Reamer Long (Small); (REF - AR-9228); Qty: 1

Arthrex Nautlius Glenoid Reamer Long (Medium); (REF - AR-9229); Qty: 1

Arthrex Nautlius Glenoid Reamer Long (Large); (REF - AR-9230); Qty: 1

Arthrex Nautlius Glenoid Reamer Long (X-Large); (REF - AR-9231); Qty: 1

Arthrex 2.8 mm Cannulated Drill Guide (Small); (REF - AR-9215-2); Qty: 1

Arthrex 2.8 mm Cannulated Drill Guide (Medium); (REF - AR-9215-4); Qty: 1

Arthrex 2.8 mm Cannulated Drill Guide (Large); (REF - AR-9215-6); Qty: 1

Arthrex 2.8 mm Cannulated Drill Guide (X-Large); (REF - AR-9215-8); Qty: 1

Arthrex Keeled Glenoid Trial (Small); (REF - AR-9217); Qty: 1

Arthrex Keeled Glenoid Trial (Medium); (REF - AR-9218); Qty: 1

Arthrex Keeled Glenoid Trial (Large); (REF - AR-9219); Qty: 1

Arthrex Keeled Glenoid Trial (X-Large); (REF - AR-9219-1); Qty: 1

Arthrex Keeled Glenoid Drill Guide (Small); (REF - AR-9215-3); Qty: 1

Arthrex Keeled Glenoid Drill Guide (Medium); (REF - AR-9215-5); Qty: 1

Arthrex Keeled Glenoid Drill Guide (Large); (REF - AR-9215-7); Qty: 1

Arthrex Keeled Glenoid Drill Guide (X-Large); (REF - AR-9215-9); Qty: 1

Arthrex Keeled Glenoid Trials & Drill Guides Caddie; (REF - AR-9225CK); Qty: 1

Arthrex Pegged Glenoid Trial (Small); (REF - AR-9236); Qty: 1

Arthrex Pegged Glenoid Trial (Medium); (REF - AR-9236-02); Qty: 1

Arthrex Pegged Glenoid Trial (Large); (REF - AR-9236-03); Qty: 1

Arthrex Pegged Glenoid Trial (X-Large); (REF - AR-9236-04); Qty: 1

Arthrex Pegged Glenoid Drill Guide (Small); (REF - AR-9231-01); Qty: 1

Arthrex Pegged Glenoid Drill Guide (Medium); (REF - AR-9231-02); Qty: 1

Arthrex Pegged Glenoid Drill Guide (Large); (REF - AR-9231-03); Qty: 1

Arthrex Pegged Glenoid Drill Guide (X-Large); (REF - AR-9231-04); Qty: 1

Arthrex Pegged Glenoid Trials & Drill Guides Caddie; (REF - AR-9225CK); Qty: 1

Arthrex Cutting Surface; (REF - AR-9205); Qty: 1

Arthrex Intramedullary (IM) Humeral Cutting Guide; (REF - AR-9401-14); Qty: 1

Arthrex Glenoid Keel Punch; (REF - AR-9214); Qty: 1

Arthrex Glenoid Reemer Drill Glove; (REF - AR-9216-2); Qty: 1

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This device has been carefully reviewed and conforms withs Prescription devices policy.

To the best of our knowledge and abilities, this device has been cleaned and handled in accordance with manufacturers instructions.

"The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not buy this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item."

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Also pers Prescription Devices Policy, we must provide the following information about our company for listings of devices that may fall under this FDA guideline:

KenMed Supply, LLC, d.b.a,

Casselberry, Florida

[phone removed by] Office Number

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