Vanguard XP® Instrumentation 32-700403
GUDID 00887868501319
Biomet Orthopedics, LLC
Surgical implant template, reusable| Primary Device ID | 00887868501319 |
| NIH Device Record Key | 128b8708-b50e-4d7e-b7ec-213d8292878d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vanguard XP® Instrumentation |
| Version Model Number | 32-700403 |
| Catalog Number | 32-700403 |
| 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 |
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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868501319 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K141407
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 |
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
[00887868501319]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-04-12 |
| Device Publish Date | 2021-04-02 |
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.