TenoLok T60A
GUDID 10845854043806
TenoLok 6.0mm Tenodesis Anchor
Conmed Corporation
Tendon/ligament bone anchor, non-bioabsorbable| Primary Device ID | 10845854043806 |
| NIH Device Record Key | c05177cf-6c3e-4a20-bd2f-78f9af83b42c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TenoLok |
| Version Model Number | T60A |
| Catalog Number | T60A |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854043806 [Primary] |
| GS1 | 20845854043803 [Package] Package: Carton [1 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K120841
FDA Product Code
| MBI | Fastener, fixation, nondegradable, soft tissue |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[10845854043806]
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Ethylene Oxide
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Ethylene Oxide
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Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-04-15 |
| Device Publish Date | 2020-11-12 |
On-Brand Devices [TenoLok]
| 10845854044711 | T60A80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
| 10845854044704 | T60S80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 8.0 mm Drill Bit |
| 10845854044681 | T60A75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
| 10845854044667 | T50S65 TenoLok Tenodesis Kit with 5.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
| 20845854044671 | Tenolok Tenodesis Kit With 5.0mm Tenolok Anchor with One #2 Hi-Fi Suture, 2.4mm Guide Pin, And 7 |
| 20845854043780 | 5.0 mm Tenolok Tenodesis Anchor with one No. 2 Hi-Fi Suture |
| 20653405987182 | T60A75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
| 20653405987175 | T60A80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
| 20653405987168 | T50S65 TenoLok Tenodesis Kit with 5.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
| 20653405987151 | T60S80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 8.0 mm Drill Bit |
| 10845854044698 | T60S75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 7.5 mm Drill Bit |
| 30845854044678 | Tenolok Tenodesis Kit With 5.0mm Tenolok Anchor with One #2 Hi-Fi Suture, 2.4mm Guide Pin, And 7 |
| 30845854043787 | 5.0 mm Tenolok Tenodesis Anchor with one No. 2 Hi-Fi Suture |
| 20653405987199 | T60S75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 7.5 mm Drill Bit |
| 10845854043806 | TenoLok 6.0mm Tenodesis Anchor |
| 10845854043790 | TenoLok 6.0 mm Tenodesis Anchor with One #2 Hi-Fi Suture |
Trademark Results [TenoLok]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TENOLOK 86719830 4948048 Live/Registered |
Conmed Corporation 2015-08-10 |
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