The following data is part of a premarket notification filed by Micro Therapeutics, Inc. D/b/a Ev3 Neurovascular with the FDA for Solitaire Platinum Revascularization Device.
| Device ID | K153071 |
| 510k Number | K153071 |
| Device Name: | Solitaire Platinum Revascularization Device |
| Classification | Catheter, Thrombus Retriever |
| Applicant | Micro Therapeutics, Inc. D/b/a Ev3 Neurovascular 9775 Toledo Way Irvine, CA 92618 |
| Contact | Phuong Chau |
| Correspondent | Phuong Chau Micro Therapeutics, Inc. D/b/a Ev3 Neurovascular 9775 Toledo Way Irvine, CA 92618 |
| Product Code | NRY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-10-22 |
| Decision Date | 2015-12-23 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00847536033955 | K153071 | 000 |
| 00847536033948 | K153071 | 000 |
| 00847536033931 | K153071 | 000 |
| 00847536020542 | K153071 | 000 |
| 00847536020535 | K153071 | 000 |
| 00847536020528 | K153071 | 000 |