The following data is part of a premarket notification filed by Biotronik Ag with the FDA for Pheron Peripheral Percutaneous Transluminal Angioplasty (pta) Catheter.
| Device ID | K052757 |
| 510k Number | K052757 |
| Device Name: | PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | BIOTRONIK AG 6024 JEAN ROAD Lake Oswego, OR 97035 |
| Contact | Jon Brumbaugh |
| Correspondent | Jon Brumbaugh BIOTRONIK AG 6024 JEAN ROAD Lake Oswego, OR 97035 |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-09-30 |
| Decision Date | 2005-10-28 |