The following data is part of a premarket notification filed by Invatec S.p.a. with the FDA for Admiral Xtreme Pta Balloon Dilatation Catheter.
Device ID | K100921 |
510k Number | K100921 |
Device Name: | ADMIRAL XTREME PTA BALLOON DILATATION CATHETER |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | INVATEC S.P.A. 3101 EMRICK BLVD Bethlehem, PA 18020 |
Contact | John Clay |
Correspondent | John Clay INVATEC S.P.A. 3101 EMRICK BLVD Bethlehem, PA 18020 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-04-02 |
Decision Date | 2010-04-30 |
Summary: | summary |