Vanguard XP® Instrumentation 32-700174
GUDID 00887868499555
Biomet Orthopedics, LLC
Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable| Primary Device ID | 00887868499555 |
| NIH Device Record Key | 962503cc-88dc-4613-af92-71043e5e16e0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vanguard XP® Instrumentation |
| Version Model Number | 32-700174 |
| Catalog Number | 32-700174 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | 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(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868499555 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K122160
FDA Product Code
| MBV | Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
[00887868499555]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-04-01 |
| Device Publish Date | 2021-03-24 |
On-Brand Devices [Vanguard XP® Instrumentation]
Trademark Results [Vanguard XP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VANGUARD XP 86148539 4642525 Live/Registered |
Biomet Manufacturing, LLC 2013-12-19 |
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