The following data is part of a premarket notification filed by Pathway Medical Technologies, Inc. with the FDA for Jetstream Navitus System; Jetstream G3 Sf System; Jetstream G3 Se System; Jetstream G3 L System.
| Device ID | K110626 |
| 510k Number | K110626 |
| Device Name: | JETSTREAM NAVITUS SYSTEM; JETSTREAM G3 SF SYSTEM; JETSTREAM G3 SE SYSTEM; JETSTREAM G3 L SYSTEM |
| Classification | Catheter, Peripheral, Atherectomy |
| Applicant | PATHWAY MEDICAL TECHNOLOGIES, INC. 10801 120TH AVENUE NE Kirkland, WA 98033 |
| Contact | Brian Cleary |
| Correspondent | Brian Cleary PATHWAY MEDICAL TECHNOLOGIES, INC. 10801 120TH AVENUE NE Kirkland, WA 98033 |
| Product Code | MCW |
| CFR Regulation Number | 870.4875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-03-04 |
| Decision Date | 2011-04-20 |
| Summary: | summary |