COR-KNOT MINI®
GUDID 10850200006077
COR-KNOT MINI® DEVICE KIT Base Package Type - Kit Each sterile package kit contains (2) single patient use COR-KNOT MINI® Devices only. Rotating shaft.
LSI Solutions, Inc.
Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable Suture clasp, non-bioabsorbable| Primary Device ID | 10850200006077 |
| NIH Device Record Key | d61b071a-be05-4066-8046-b6cf0df9a9f4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | COR-KNOT MINI® |
| Version Model Number | 031300 |
| Company DUNS | 603420183 |
| Company Name | LSI Solutions, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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
| Outer Diameter | 4 Millimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Outer Diameter | 4 Millimeter |
| Length | 17 Centimeter |
| Length | 17 Centimeter |
| Length | 17 Centimeter |
| Length | 17 Centimeter |
| Length | 17 Centimeter |
| Length | 17 Centimeter |
| Length | 17 Centimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850200006070 [Primary] |
| GS1 | 10850200006077 [Package] Contains: 00850200006070 Package: Case [6 Units] In Commercial Distribution |
| GS1 | 40850200006078 [Unit of Use] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K100593
FDA Product Code
| HCF | Instrument, Ligature Passing And Knot Tying |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
[10850200006077]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-02-04 |
On-Brand Devices [COR-KNOT MINI®]
| 10850200006299 | COR-KNOT MINI® COMBO KIT Base Package Type - Kit Each sterile package kit contains (2) single p |
| 10850200006084 | COR-KNOT MINI® COMBO KIT Base Package Type - Kit Each sterile package kit contains (2) single p |
| 10850200006077 | COR-KNOT MINI® DEVICE KIT Base Package Type - Kit Each sterile package kit contains (2) single |
Trademark Results [COR-KNOT MINI]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 COR-KNOT MINI 86192506 4697145 Live/Registered |
LSI Solutions, Inc. 2014-02-13 |
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