The following data is part of a premarket notification filed by Stryker with the FDA for Stryker 90-s Max Serfas Energy Probe.
| Device ID | K171391 |
| 510k Number | K171391 |
| Device Name: | Stryker 90-S Max SERFAS Energy Probe |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | Stryker 5900 Optical Court San Jose, CA 95138 |
| Contact | Ben Krebs |
| Correspondent | Ben Krebs Stryker 5900 Optical Court San Jose, CA 95138 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-05-11 |
| Decision Date | 2018-01-26 |
| Summary: | summary |