The following data is part of a premarket notification filed by Orbusneich Medical Trading, Inc. with the FDA for Scoreflex Pta Scoring Balloon Catheter.
Device ID | K182713 |
510k Number | K182713 |
Device Name: | Scoreflex PTA Scoring Balloon Catheter |
Classification | Catheter, Percutaneous, Cutting/scoring |
Applicant | OrbusNeich Medical Trading, Inc. 5363 NW 35th Avenue Fort Lauderdale, FL 33309 |
Contact | John Pazienza |
Correspondent | John Pazienza OrbusNeich Medical Trading, Inc. 5363 NW 35th Avenue Fort Lauderdale, FL 33309 |
Product Code | PNO |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-27 |
Decision Date | 2019-06-11 |