| Primary Device ID | B504OMG01009010 |
| NIH Device Record Key | 7c01c659-7364-4a38-a5b6-0c7f1e27fbf3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | In2Bones |
| Version Model Number | G01 00901 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | false |
| 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 | B504OMG01009010 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-23 |
| Device Publish Date | 2024-02-15 |
| B504OMP06N06810 | P06 N0681 |
| B504OMP06N03330 | P06 N0333 |
| B504OMP04N02210 | P04 N0221 |
| B504OMG01009010 | G01 00901 |
| B504OMG01008910 | G01 00891 |
| B504OMBP07N00310 | P07 N0031 |
| B504OMP06N04520 | P06 N0452 |
| B504OMG05S10080 | G05 S1008 |
| B504OMP06N07110 | P06 N0711 |
| B504OMAR1980R05S0 | AR-1980R-05S |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() IN2BONES 79112849 4344702 Live/Registered |
IN2BONES 2012-02-07 |