Admiral AP1-200020
GUDID 10889981238162
Cervical Plate, 2 Level, 20mm
SEASPINE ORTHOPEDICS CORPORATION
Spinal fixation plate, non-bioabsorbable| Primary Device ID | 10889981238162 |
| NIH Device Record Key | b9b244a7-25f0-44ff-9044-7b0eef4cddf6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Admiral |
| Version Model Number | AP1-200020 |
| Catalog Number | AP1-200020 |
| Company DUNS | 079840876 |
| Company Name | SEASPINE ORTHOPEDICS CORPORATION |
| 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 | 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(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10889981238162 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K202064
FDA Product Code
| KWQ | Appliance, fixation, spinal intervertebral body |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
[10889981238162]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-16 |
| Device Publish Date | 2020-12-08 |
On-Brand Devices [Admiral]
| 10889981247683 | Streamline Handle, Orange, Spin Top |
| 10889981239831 | 4.3mm Screw Caddy |
| 10889981239824 | 4.0mm Screw Caddy |
| 10889981239817 | Temporary Fixation Caddy |
| 10889981239800 | Trial Drill Guide Caddy |
| 10889981239794 | 5 Level Plate Caddy |
| 10889981239787 | 4 Level Plate Caddy |
| 10889981239770 | 3 Level Plate Caddy |
| 10889981239763 | 2 Level Plate Caddy |
| 10889981239756 | 1 Level Plate Caddy |
| 10889981239749 | ACP Misc Tray (4/5 Level Plate & Misc Tray) |
| 10889981239732 | ACP Fixation Tray (Prep & Insertion Tray) |
| 10889981239725 | ACP Implant Tray (Plate & Screw Tray) |
| 10889981239718 | ACP Tray Case |
| 10889981239596 | Cervical Plate, 3 Level, 78mm |
| 10889981239589 | Cervical Plate, 3 Level, 75mm |
| 10889981239572 | Cervical Plate, 3 Level, 72mm |
| 10889981239565 | Cervical Plate, 3 Level, 69mm |
| 10889981239558 | Cervical Plate, 3 Level, 66mm |
| 10889981239541 | Cervical Plate, 3 Level, 63mm |
| 10889981239534 | Cervical Plate, 3 Level, 57mm |
| 10889981239527 | Cervical Plate, 3 Level, 51mm |
| 10889981239510 | Cervical Plate, 3 Level, 45mm |
| 10889981239503 | Cervical Plate, 3 Level, 39mm |
| 10889981239497 | Plate Length Caliper, 52-80mm |
| 10889981239473 | Temporary Fixation Pin |
| 10889981239459 | Plate Length Caliper, 8-52mm |
| 10889981239442 | Plate Holder |
| 10889981239435 | Trial Drill Guide, 12mm |
| 10889981239428 | Trial Drill Guide, 11mm |
| 10889981239411 | Trial Drill Guide, 10mm |
| 10889981239404 | Trial Drill Guide, 9mm |
| 10889981239398 | Trial Drill Guide, 8mm |
| 10889981239381 | Trial Drill Guide, 7mm |
| 10889981239374 | Trial Drill Guide, 6mm |
| 10889981239367 | Trial Drill Guide, 5mm |
| 10889981239350 | Trial Drill Guide Inserter |
| 10889981239343 | Drill, 20mm |
| 10889981239336 | Drill, 18mm |
| 10889981239329 | Drill, 16mm |
| 10889981239312 | Drill, 14mm |
| 10889981239305 | Drill, 12mm |
| 10889981239299 | Drill, 10mm |
| 10889981239282 | Self Guiding Awl, 10mm, Variable |
| 10889981239275 | Awl, 10mm |
| 10889981239268 | Lateral DTS Guide, 15 Deg |
| 10889981239251 | Midline DTS Guide, 0, 15, 25 Deg |
| 10889981239244 | Drill Guide, Double Barrel, Variable |
| 10889981239237 | Lateral DTS Guide, 0 Deg |
| 10889981239220 | Drill Guide, Fixed |
Trademark Results [Admiral]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ADMIRAL 98578097 not registered Live/Pending |
Polygroup North America, Inc. 2024-05-31 |
 ADMIRAL 98184983 not registered Live/Pending |
LPI CONSUMER PRODUCTS, INC. 2023-09-18 |
 ADMIRAL 97740100 not registered Live/Pending |
Spectrum Paint Company, Inc. 2023-01-03 |
 ADMIRAL 97462465 not registered Live/Pending |
Admiral Corporation of America, Inc. 2022-06-16 |
 ADMIRAL 97462448 not registered Live/Pending |
Admiral Corporation of America, Inc. 2022-06-16 |
 ADMIRAL 97462422 not registered Live/Pending |
Admiral Corporation of America, Inc. 2022-06-16 |
 ADMIRAL 97072381 not registered Live/Pending |
California Exotic Novelties, LLC 2021-10-13 |
 ADMIRAL 97072374 not registered Live/Pending |
California Exotic Novelties, LLC 2021-10-13 |
 ADMIRAL 97072368 not registered Live/Pending |
California Exotic Novelties, LLC 2021-10-13 |
 ADMIRAL 90789826 not registered Live/Pending |
Admiral Corporation of America, Inc. 2021-06-23 |
 ADMIRAL 90607242 not registered Live/Pending |
Admiral Corporation of America, Inc. 2021-03-27 |
 ADMIRAL 90545605 not registered Live/Pending |
Bulletproof Property Management, LLC 2021-02-24 |
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