ENDOSKELETON Posterior DPK 1100-0021

GUDID M682110000210

Down, Pituitary Rongeur, 4mm, 10in Long

TITAN SPINE, LLC

Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur Orthopaedic joint/limb rongeur

• Primary Device ID: M682110000210
• NIH Device Record Key: 0fceec47-64cc-4bfd-a6d3-ab78bb718192
• Commercial Distribution Discontinuation: 2020-09-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ENDOSKELETON Posterior DPK
• Version Model Number: 1100-0021
• Catalog Number: 1100-0021
• Company DUNS: 623316978
• Company Name: TITAN SPINE, LLC
• Device Count: 1
• DM Exempt: true
• 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: true
• 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

• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M682110000210 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

[M682110000210]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-09-22
• 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