PHALINX 45A01013

GUDID 00889797102193

Solid Angled

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 00889797102193
• NIH Device Record Key: fac7c64f-9b58-4003-9d4d-6ae94da30bf0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PHALINX
• Version Model Number: 45A01013
• Catalog Number: 45A01013
• Company DUNS: 807201207
• Company Name: WRIGHT MEDICAL TECHNOLOGY, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com

Device Dimensions

• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree
• Device Size Text, specify: 0
• Angle: 10 degree

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889797102193 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K212996

FDA Product Code

• HTY: PIN, FIXATION, SMOOTH

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-22
• Device Publish Date: 2022-11-14

On-Brand Devices [PHALINX]

• 00840420166173: 05-053
• 00840420166166: RETIRED
• 00840420166159: 05-051
• 00840420166142: RETIRED
• 00840420166135: 05-043
• 00840420166128: RETIRED
• 00840420166111: RETIRED
• 00840420166104: RETIRED
• 00840420166098: 45301014
• 00840420166081: 45301013
• 00840420166074: 45301012
• 00840420166067: 45301011
• 00840420166050: 45301004
• 00840420166043: 45301003
• 00840420166036: 45301002
• 00840420166029: 45301001
• 00889797060332: Hammertoe Drill
• 00889797060325: Hammertoe Drill
• 00889797060318: Hammertoe Drill
• 00889797060301: Hammertoe Drill
• 00889797060295: Hammertoe Drill
• 00889797060288: Hammertoe Drill
• 00889797060271: Hammertoe Drill
• 00889797060264: Hammertoe Drill
• 00889797060257: Hammertoe K-Wire
• 00889797060240: Hammertoe K-Wire
• 00889797060233: K-Wire
• 00889797037655: Screw Pickup Forceps
• 00889797013826: Hammertoe Implant Impactor
• 00889797013819: Hammertoe Drill Handle
• 00889797013802: Hammertoe Implant Pickup Forceps
• 00889797013796: Hammertoe Handle
• 00889797013789: Hammertoe Handle
• 00889797013772: Hammertoe Handle
• 00889797013765: Hammertoe Handle
• 00889797013758: Hammertoe Handle
• 00889797013741: Hammertoe Handle
• 00889797013734: Hammertoe Handle
• 00889797013727: Hammertoe Handle
• 00889797102209: Solid Angled
• 00889797102193: Solid Angled
• 00889797102186: Solid Angled
• 00889797102179: Solid Angled
• 00889797102162: Cannulated Straight
• 00889797102155: Cannulated Straight
• 00889797102148: Cannulated Straight
• 00889797102131: Cannulated Straight