A.L.P.S.® CLAVICLE PLATING SYSTEMDRILL BIT 233500022
GUDID 00880304834743
Biomet Orthopedics, LLC
Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable| Primary Device ID | 00880304834743 |
| NIH Device Record Key | fb7d8165-ffab-4eb3-9f02-49a20dd2f4e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | A.L.P.S.® CLAVICLE PLATING SYSTEMDRILL BIT |
| Version Model Number | 233500022 |
| Catalog Number | 233500022 |
| 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
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 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 | 00880304834743 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K173767
FDA Product Code
| HRS | Plate, fixation, bone |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
[00880304834743]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-09-20 |
| Device Publish Date | 2019-02-08 |
On-Brand Devices [A.L.P.S.® CLAVICLE PLATING SYSTEMDRILL BIT]
| 00880304834750 | 233500027 |
| 00880304834743 | 233500022 |
Trademark Results [A.L.P.S.]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 A.L.P.S. 86414170 not registered Dead/Abandoned |
Biomet C.V. 2014-10-03 |
 A.L.P.S. 86122580 4795950 Live/Registered |
Biomet C.V. 2013-11-19 |
 A.L.P.S. 85887976 not registered Dead/Abandoned |
Biomet C.V. 2013-03-27 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.