Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Micrus Endovascular Corporation · Predicate Candidate Screening
23 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
40 daysmedian FDA review time
138 days90th percentile
23clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K103780 | MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM; MICRUS ASCE | Micrus Endovascular Corporation | 2011-01-26 | 30 | 0 |
| K102818 | MICRUS ONE 2 ONE GUIDEWIRE, MICRUS ONE 2 ONE SOFT GUIDEWIRE | Micrus Endovascular Corporation | 2010-12-03 | 66 | 0 |
| K092702 | MICRUS MICROCATHETER, MODEL COURIER 270 | Micrus Endovascular Corporation | 2009-11-20 | 79 | 0 |
| K091504 | MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7MM,6X9MM, MICRUS | Micrus Endovascular Corporation | 2009-06-19 | 29 | 0 |
| K083922 | MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00 | Micrus Endovascular Corporation | 2009-05-06 | 126 | 0 |
| K090274 | MICRUS ONE 2 ONE GUIDEWIRE AND SOFT GUIDEWIRE | Micrus Endovascular Corporation | 2009-03-03 | 27 | 0 |
| K083646 | MICRUS MICROCOLI SYSTEM, DELTAPLUSH, MODELS CPL, DPL | Micrus Endovascular Corporation | 2009-01-02 | 24 | 1 |
| K082739 | MICRUS MICROCOIL DELIVERY SYSTEM | Micrus Endovascular Corporation | 2008-10-17 | 29 | 0 |
| K080861 | MICRUS ASCENT OCCLUSION BALLOON CATHETER | Micrus Endovascular Corporation | 2008-08-27 | 153 | 0 |
| K080379 | MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 STRETCH RESISTANT | Micrus Endovascular Corporation | 2008-06-30 | 138 | 0 |
| K080437 | MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF | Micrus Endovascular Corporation | 2008-05-08 | 83 | 0 |
| K073442 | MICRUS MICROCOIL SYSTEMS | Micrus Endovascular Corporation | 2008-02-26 | 81 | 0 |
| K072173 | MICRUS MICROCOIL SYSTEM CASHMERE-CERECYTE, MODEL CRC; CASHME | Micrus Endovascular Corporation | 2007-10-05 | 60 | 1 |
| K072526 | MICRUS COURIER ENZO MICROCATHETER 0.0190 | Micrus Endovascular Corporation | 2007-10-05 | 28 | 0 |
| K071246 | MICRUS MICROCOIL DELIVERY SYSTEM, MODELS SPH, HEL, CHE, PC4, | Micrus Endovascular Corporation | 2007-06-01 | 29 | 0 |
| K070456 | MICRUS COURIER ENZO MICROCATHETER 0.017 | Micrus Endovascular Corporation | 2007-05-24 | 97 | 0 |
| K070707 | MICRUS MICROCOIL SYSTEM | Micrus Endovascular Corporation | 2007-04-06 | 23 | 0 |
| K063653 | MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC | Micrus Endovascular Corporation | 2007-01-17 | 40 | 0 |
| K062036 | MICRUS MICROCOIL SYSTEM PRESIDIO-18, MODEL PC4 | Micrus Endovascular Corporation | 2006-08-25 | 37 | 1 |
| K061963 | MICRUS MICROCATHETER COURIER PRE-SHAPED, MODELS MPS170045-00 | Micrus Endovascular Corporation | 2006-08-04 | 23 | 0 |
| K060116 | MICRUS COURIER MICROCATHETERS | Micrus Endovascular Corporation | 2006-05-12 | 115 | 0 |
| K053265 | MICRUS GUIDE WIRE, WATUSI 0.014 | Micrus Endovascular Corporation | 2006-04-28 | 157 | 1 |
| K053160 | MICRUS MODIFIED MICROCOIL 18-SYSTEM, CERECYTE, MODEL CSP & C | Micrus Endovascular Corporation | 2005-12-07 | 23 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda