The following data is part of a premarket notification filed by Meadox Medicals, Div. Boston Scientific Corp. with the FDA for Meadox Szilagyi Graft.
Device ID | K810376 |
510k Number | K810376 |
Device Name: | MEADOX SZILAGYI GRAFT |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | MEADOX MEDICALS, DIV. BOSTON SCIENTIFIC CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | DSY |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-02-12 |
Decision Date | 1981-03-05 |