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PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER

Page Type
Cleared 510(K)
510(k) Number
K052757
510(k) Type
Special
Applicant
BIOTRONIK AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2005
Days to Decision
28 days
Submission Type
Summary

PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER

Page Type
Cleared 510(K)
510(k) Number
K052757
510(k) Type
Special
Applicant
BIOTRONIK AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2005
Days to Decision
28 days
Submission Type
Summary