| Primary Device ID | 07613327263107 |
| NIH Device Record Key | b00d87f0-0f52-4165-b0d2-a9c34f3915c2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | XIA ANTERIOR |
| Version Model Number | 48040245 |
| Catalog Number | 48040245 |
| Company DUNS | 149183167 |
| Company Name | Stryker Corporation |
| 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 | 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 Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327263107 [Primary] |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327263107]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-26 |
| Device Publish Date | 2018-09-24 |
| 07613327276572 | BENDING IRON, LEFT |
| 07613327276503 | BENDING IRON, RIGHT |
| 07613327263299 | INSERTER TUBE |
| 07613327263107 | SCREWDRIVER |
| 07613327263091 | CROSS CONNECTOR HOLDER |
| 07613327263084 | CALIPER |
| 07613327263077 | PARALLEL COMPRESSOR |
| 07613327263060 | DUAL STAPLE IMPACTOR |
| 07613327263046 | ANGLED AWL |
| 07613327263039 | PARALLEL DISTRACTER |
| 07613327119886 | TITANIUM IMPLANT CONTAINER LID |
| 07613327119862 | SCREW RACK |
| 07613327118919 | ANTERIOR LP INSTRUMENT CONTAINER |
| 07613327118896 | TITANIUM IMPLANT CONTAINER |