| Primary Device ID | 07613327065152 |
| NIH Device Record Key | cf11a31f-972f-46b3-8b27-1528de68e667 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NAVIGATED MANTIS |
| Version Model Number | 48765300 |
| Catalog Number | 48765300 |
| Company DUNS | 149183167 |
| Company Name | Stryker Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| 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 |
|---|---|
| GS1 | 07613327065152 [Primary] |
| OLO | Orthopedic stereotaxic instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327065152]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |
| 07613327121537 | TRAY |
| 07613327065190 | T-HANDLE RATCHET |
| 07613327065183 | POLYAXIAL SCREWDRIVER |
| 07613327065176 | CANNULATED AWL |
| 07613327065169 | POLYAXIAL SCREWDRIVER |
| 07613327065152 | TAP SLEEVE |
| 07613327065145 | CANNULATED TAP |
| 07613327065138 | CANNULATED TAP |
| 07613327065121 | CANNULATED TAP |
| 07613327065114 | CANNULATED TAP |
| 07613327065107 | CANNULATED TAP |