K2M General Instruments PRO-1124-01

GUDID 10888857531178

Quick Connect Adapter

K2M, INC.

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 10888857531178
• NIH Device Record Key: 153eb8d7-9b14-4935-9ee1-4b55dc20a7ae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K2M General Instruments
• Version Model Number: PRO-1124-01
• Catalog Number: PRO-1124-01
• Company DUNS: 146060863
• Company Name: K2M, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com
• Phone: +1(571)919-2000
• Email: mark.zellers@stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10888857531178 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

[10888857531178]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-09-23
• Device Publish Date: 2021-09-15

On-Brand Devices [K2M General Instruments]

• 10888857467521: Lamina Spreader
• 10888857466104: Lamina Spreader
• 10888857465763: Offset Lamina Spreader
• 10888857468306: Spreader
• 10888857463523: Pusher, ALIF
• 10888857463400: Down Curette Bayoneted, Size #3
• 10888857463394: Up Curette Bayoneted, Size #3
• 10888857463387: Reverse Angled Curette Bayoneted, Size #3
• 10888857463370: Right Angled Curette Bayoneted, Size #3
• 10888857463363: Left Angled Curette Bayoneted, Size #3
• 10888857463356: Left Facing Curette Bayoneted, Size #3
• 10888857463349: Right Facing Curette Bayoneted, Size #3
• 10888857463332: Down Serrated Curette Bayoneted, Size #3
• 10888857463325: Up Serrated Curette Bayoneted, Size #3
• 10888857463318: Angled Teardrop Curette Bayoneted,
• 10888857463301: Teardrop Curette Bayoneted
• 10888857463295: Angled Ring Curette Bayoneted
• 10888857463288: Ring Curette, Bayoneted
• 10888857435445: Integrated Graft Ramps, Size 22 mm
• 10888857435438: Integrated Graft Ramps, Size 18 mm
• 10888857432406: Lordotic Modular Trial, Size 22x60x16 mm, 12°
• 10888857432390: Lordotic Modular Trial, Size 22x60x14 mm, 12°
• 10888857432383: Lordotic Modular Trial, Size 22x60x12 mm, 12°
• 10888857432376: Lordotic Modular Trial, Size 22x60x10 mm, 12°
• 10888857432369: Silicone T-Handle with Strike Plate,
• 10888857431058: End Plate Rasp
• 10888857429871: Lordotic Modular Trial, Size 22x60x16 mm, 15°
• 10888857429864: Lordotic Modular Trial, Size 22x60x14 mm, 15°
• 10888857429857: Lordotic Modular Trial, Size 22x60x12 mm, 15°
• 10888857429840: Lordotic Modular Trial, Size 22x60x16 mm, 8°
• 10888857429833: Lordotic Modular Trial, Size 22x60x14 mm, 8°
• 10888857429826: Lordotic Modular Trial, Size 22x60x12 mm, 8°
• 10888857429819: Lordotic Modular Trial, Size 22x60x10 mm, 8°
• 10888857429802: Lordotic Modular Trial, Size 22x60x08 mm, 8°
• 10888857429796: Parallel Modular Trial, Size 22x60x16 mm, 0°
• 10888857429789: Parallel Modular Trial, Size 22x60x14 mm, 0°
• 10888857429772: Parallel Modular Trial, Size 22x60x12 mm, 0°
• 10888857429765: Parallel Modular Trial, Size 22x60x10 mm, 0°
• 10888857429758: Parallel Modular Trial, Size 22x60x08 mm, 0°
• 10888857427747: Angled Disc Wedge, Size 4-6 mm
• 10888857427730: Angled Disc Wedge, Size 3-5 mm
• 10888857427723: Disc Wedge, Size 4-6 mm
• 10888857427716: Disc Wedge, Size 3-5 mm
• 10888857427709: Stirrup Curette
• 10888857423176: 18 mm Lateral Box Chisel, Size 18x8 mm
• 10888857423169: 18 mm Lateral Box Chisel, Size 18x6 mm
• 10888857423152: 18 mm Lateral Box Chisel, Size 18x4 mm
• 10888857423145: Trial Rasp, Size 18x60x10 mm
• 10888857423138: Trial Rasp, Size 18x60x8 mm
• 10888857423121: Trial Rasp, Size 18x60x6 mm