| Primary Device ID | B504OM2460020 |
| NIH Device Record Key | 39755c9c-a4d8-44a6-9291-7afdba3e5890 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Crossroads |
| Version Model Number | 246002 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504OM2460020 [Primary] |
| HTO | Reamer |
| HTW | Bit, Drill |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-24 |
| Device Publish Date | 2024-05-16 |
| B504OM710025000 | 7100-2500 |
| B504OM710020000 | 7100-2000 |
| B504OM710018000 | 7100-1800 |
| B504OM710015000 | 7100-1500 |
| B504OM700040SB0 | 7000-40SB |
| B504OM2460020 | 246002 |
| B504OM2470020 | 247002 |
| B504OM2451100 | 245110 |
| B504OM2451070 | 245107 |
| B504OM2451060 | 245106 |
| B504OM2450660 | 245066 |
| B504OM2450650 | 245065 |
| B504OM2450560 | 245056 |
| B504OM2450550 | 245055 |
| B504OM1305170 | 130517 |
| B504OM1305050 | 130505 |
| B504OM1305040 | 130504 |
| B504OM1305030 | 130503 |
| B504OM1212250 | 121225 |
| B504OM150047010 | 1500-4701 |
| B504OM1305280 | 130528 |
| B504OM1305000 | 130500 |