The following data is part of a premarket notification filed by Kaneka Corporation with the FDA for Crosstella Otw.
Device ID | K160004 |
510k Number | K160004 |
Device Name: | Crosstella OTW |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | KANEKA CORPORATION 1-12-32, AKASAKA, MINATO-KU Tokyo, JP 107-6025 |
Contact | Toshihiko Motomine |
Correspondent | Christopher M. Sloan QUINTILES CONSULTING 1801 ROCKVILLE PIKE SUITE 300 Rockville, MD 20852 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-01-04 |
Decision Date | 2016-04-29 |
Summary: | summary |