The following data is part of a premarket notification filed by Micro Therapeutics, Inc. with the FDA for Fx Detachable Coil System.
| Device ID | K060747 |
| 510k Number | K060747 |
| Device Name: | FX DETACHABLE COIL SYSTEM |
| Classification | Device, Neurovascular Embolization |
| Applicant | MICRO THERAPEUTICS, INC. 2 GOODYEAR Irvine, CA 92618 |
| Contact | Florin Truuvert |
| Correspondent | Florin Truuvert MICRO THERAPEUTICS, INC. 2 GOODYEAR Irvine, CA 92618 |
| Product Code | HCG |
| CFR Regulation Number | 882.5950 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-03-20 |
| Decision Date | 2007-04-24 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00836462011045 | K060747 | 000 |
| 20763000290706 | K060747 | 000 |