The following data is part of a premarket notification filed by Micrus Endovascular Corporation with the FDA for Micrus Microcoil System Cashmere-cerecyte, Model Crc; Cashmere-sr, Model Src.
Device ID | K072173 |
510k Number | K072173 |
Device Name: | MICRUS MICROCOIL SYSTEM CASHMERE-CERECYTE, MODEL CRC; CASHMERE-SR, MODEL SRC |
Classification | Device, Neurovascular Embolization |
Applicant | MICRUS ENDOVASCULAR CORPORATION 821 FOX LANE San Jose, CA 95131 |
Contact | Patrick Lee |
Correspondent | Patrick Lee MICRUS ENDOVASCULAR CORPORATION 821 FOX LANE San Jose, CA 95131 |
Product Code | HCG |
CFR Regulation Number | 882.5950 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-08-06 |
Decision Date | 2007-10-05 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00878528004578 | K072173 | 000 |
00878528004417 | K072173 | 000 |
00878528004424 | K072173 | 000 |
00878528004448 | K072173 | 000 |
00878528004455 | K072173 | 000 |
00878528004462 | K072173 | 000 |
00878528004486 | K072173 | 000 |
00878528004493 | K072173 | 000 |
00878528004530 | K072173 | 000 |
00878528004400 | K072173 | 000 |