For Sale STRYKER 6003-300-031 6003-300-041 6003-12 Navigation Smart Instruments Tray

MPN: 6003-300-031 6003-300-041 6003-12
Stryker Navigation Instruments Tray 6003-300-031 6003-300-041 6003-12 6007-530-000 6003-300-010 6541-4-401 6003-027-000 6007-015-000 6003-100-100 6003-100-090 6003-100-020 6003-010-000 6003-005-000This Stryker Navigation Instruments Tray 6003-300-031 6003-300-041 6003-12 6007-530-000 6003-300-010 6541-4-401 6003-027-000 6007-015-000 6003-100-100 6003-100-090 6003-100-020 6003-010-000 6003-005-000 is in great working and cosmetic condition.

What's Included:

Aesculap, Sterilization Tray; (REF) Qty: 1

Stryker, ASM Fixation Plate, Extension A; (REF 6003-300-031) Qty: 1

Stryker, ASM Fixation Plate, Extension B; (REF 6003-300-041) Qty: 1

Stryker, Precision Navigation Orthopedic Hand Piece; (REF 6003-12) Qty: 1

Stryker, Anchoring Pin, 5mm x 30mm; (REF 6007-530-000) Qty: 2

Stryker, Mini Cutting Guide; (REF 6003-300-010) Qty: 1

Stryker, Navigation Tracker Adapter; (REF 6541-4-401) Qty: 1

Stryker, Resection Plane Probe, Slots 1.3mm; (REF 6003-027-000) Qty: 1

Stryker, Navigation Insertion Tool; (REF 6007-015-000) Qty: 1

Stryker, Screwdriver; (REF 6003-100-100) Qty: 1

Stryker, Tracker Adapter; (REF 6003-100-090) Qty: 1

Stryker, Adjustment Component; (REF 6003-100-020) Qty: 1

Stryker, Femoral Tracker; (REF 6003-010-000) Qty: 1

Stryker, Tibial/Pelvic Tracker; (REF 6003-005-000) 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:

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