Vanguard XP® Instrumentation 32-700291
GUDID 00887868500510
Biomet Orthopedics, LLC
Surgical implant template, reusable| Primary Device ID | 00887868500510 |
| NIH Device Record Key | b9cde84d-73bb-4d58-b71d-4eed17a8c489 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vanguard XP® Instrumentation |
| Version Model Number | 32-700291 |
| Catalog Number | 32-700291 |
| 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 | 00887868500510 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K122160
FDA Product Code
| OIY | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
Moist Heat or Steam Sterilization
[00887868500510]
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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