PROPELLER HEAD 982028
GUDID 00880304416826
Biomet Orthopedics, LLC
Orthopaedic bone screw, non-bioabsorbable, sterile| Primary Device ID | 00880304416826 |
| NIH Device Record Key | ef1a7b70-0789-41b6-9507-51f6b6ad42e2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PROPELLER HEAD |
| Version Model Number | 982028 |
| Catalog Number | 982028 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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
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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304416826 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K024086
FDA Product Code
| HWC | Screw, fixation, bone |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-06-23 |
| Device Publish Date | 2015-10-24 |
Devices Manufactured by Biomet Orthopedics, LLC
| 00880304858992 - JUGGERKNOT | 2025-09-22 |
| 00880304404809 - MINI RC NEEDLE | 2025-09-08 |
| 00887868571718 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571725 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571732 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571749 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571756 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571763 - RingLoc®+ Triflange | 2025-06-20 |
Trademark Results [PROPELLER HEAD]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PROPELLER HEAD 85585256 not registered Dead/Abandoned |
Terravant Wine Company, LLC 2012-03-30 |
 PROPELLER HEAD 75875059 not registered Dead/Abandoned |
Burdick, Jonathan R. 1999-12-27 |
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