PROSTEP HVS03014

GUDID 00889797072496

HV Screw

WRIGHT MEDICAL TECHNOLOGY, INC.

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

• Primary Device ID: 00889797072496
• NIH Device Record Key: a304b88e-f966-40df-b997-912f5cab9487
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROSTEP
• Version Model Number: HVS03014
• Catalog Number: HVS03014
• Company DUNS: 807201207
• Company Name: WRIGHT MEDICAL TECHNOLOGY, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: true
• 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(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

• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter
• Length: 14 Millimeter
• Outer Diameter: 3 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889797072496 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170889

FDA Product Code

• HWC: Screw, fixation, bone

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: 2022-12-13
• Device Publish Date: 2022-12-05

On-Brand Devices [PROSTEP]

• 00889797071970: MIS Sterile Instrument Pack w/ Blade & Burr
• 00889797071956: MIS Sterile Instrument Pack
• 00889797072625: HV Screw
• 00889797072618: HV Screw
• 00889797072601: HV Screw
• 00889797072595: HV Screw
• 00889797072588: HV Screw
• 00889797072571: HV Screw
• 00889797072564: HV Screw
• 00889797072557: HV Screw
• 00889797072540: HV Screw
• 00889797072533: HV Screw
• 00889797072526: HV Screw
• 00889797072519: HV Screw
• 00889797072502: HV Screw
• 00889797072496: HV Screw
• 00889797072489: HV Screw
• 00889797072472: HV Screw