ENDOSKELETON Posterior DPK 1100-0008

GUDID M682110000080

Straight, Up, Bayonet, Cup Curette, Small

TITAN SPINE, LLC

Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable

• Primary Device ID: M682110000080
• NIH Device Record Key: e5daaed8-6c1c-4b57-9bc7-1076f6effc25
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ENDOSKELETON Posterior DPK
• Version Model Number: 1100-0008
• Catalog Number: 1100-0008
• Company DUNS: 623316978
• Company Name: TITAN SPINE, LLC
• 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(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com
• Phone: +1(262)242-7801
• Email: productinfo@titanspine.com

Device Dimensions

• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch
• Device Size Text, specify: 0
• Length: 15 Inch

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M682110000080 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

[M682110000080]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-05-07
• Device Publish Date: 2016-09-17

On-Brand Devices [ENDOSKELETON Posterior DPK]

• M682110000160: Lateral Angled, Bayonet, Ring Curette, 7mm
• M682110000150: Angled Up, Bayonet, Ring Curette, 7mm
• M682110000140: Straight, Bayonet, Ring Curette, 7mm
• M682110000120: Straight, Up, Bayonet, Cup Curette, Large
• M682110000110: 90 Deg Reverse Angle (Push), Bayonet, Cup Curette, Medium
• M682110000100: Straight, Down, Bayonet, Cup Curette, Medium
• M682110000090: Straight, Up, Bayonet, Cup Curette, Medium
• M682110000080: Straight, Up, Bayonet, Cup Curette, Small
• M682110000250: INSTRUMENT TRAY SYSTEM
• M682110000230: Nerve Root Retractor, 10mm, X-Large
• M682110000220: Lamina Spreader, Large
• M682110000210: Down, Pituitary Rongeur, 4mm, 10in Long
• M682110000200: Up, Pituitary Rongeur, 4mm, 10in Long
• M682110000190: Straight, Pituitary Rongeur, 4mm, 10in Long
• M682110000180: Kerrison Rongeur, 4mm, 8in Long
• M682110000170: Kerrison Rongeur, 3mm, 8in Long
• M682110000130: Bayonet, Long Osteotome, 6mm