The following data is part of a premarket notification filed by Philips Medical Stystems Nederland Bv with the FDA for Stentboost Live.
| Device ID | K170144 |
| 510k Number | K170144 |
| Device Name: | StentBoost Live |
| Classification | Interventional Fluoroscopic X-ray System |
| Applicant | Philips Medical Stystems Nederland BV Veenpluis 4-6 Best, NL 5684pc |
| Contact | Elaine Alan |
| Correspondent | Elaine Alan Philips Medical Stystems Nederland BV Veenpluis 4-6 Best, NL 5684pc |
| Product Code | OWB |
| CFR Regulation Number | 892.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-01-17 |
| Decision Date | 2017-06-07 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838080812 | K170144 | 000 |
| 00884838101890 | K170144 | 000 |