| Primary Device ID | M695150020130 |
| NIH Device Record Key | bd0d74b6-5843-44b8-95ef-16bcd6e1ae6d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GEO Hammertoe |
| Version Model Number | 15002013 |
| Catalog Number | 15002013 |
| Company DUNS | 010968002 |
| Company Name | Tyber Medical LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Phone | +1(866)761-0933 |
| ksimpkins@tybermed.com | |
| Phone | +1(866)761-0933 |
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| Phone | +1(866)761-0933 |
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| ksimpkins@tybermed.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M695150020130 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-01-17 |
| Device Publish Date | 2019-08-23 |
| M695150230150 | TyFix Cannulated Ø3.0mm x 15mm |
| M695150225150 | TyFix Cannulated Ø2.5mm x 15mm |
| M695150220130 | TyFix Cannulated Ø2.0mm x 13mm |
| M695150130150 | TyFix Solid 10° Ø3.0mm x 15mm |
| M695150125150 | TyFix Solid 10° Ø2.5mm x 15mm |
| M695150120130 | TyFix Solid 10° Ø2.0mm x 13mm |
| M695150030150 | TyFix Solid 0° Ø3.0mm x 15mm |
| M695150025150 | TyFix Solid 0° Ø2.5mm x 15mm |
| M695150020130 | TyFix Solid 0° Ø2.0mm x 13mm |