The following data is part of a premarket notification filed by Stryker Sustainability Solutions with the FDA for Reprocessed Ligasure Maryland Jaw Sealer/divider.
| Device ID | K180499 |
| 510k Number | K180499 |
| Device Name: | Reprocessed LigaSure Maryland Jaw Sealer/Divider |
| Classification | Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed |
| Applicant | Stryker Sustainability Solutions 1810 W Drake Drive Tempe, AZ 85283 |
| Contact | Scott English |
| Correspondent | Scott English Stryker Sustainability Solutions 1810 W Drake Drive Tempe, AZ 85283 |
| Product Code | NUJ |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-02-26 |
| Decision Date | 2018-04-23 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 57613327375812 | K180499 | 000 |
| 57613327375805 | K180499 | 000 |
| 57613327375799 | K180499 | 000 |
| 57613327504908 | K180499 | 000 |
| 57613327504892 | K180499 | 000 |
| 57613327504885 | K180499 | 000 |