FDA 510(k) Applications Submitted by STD MFG., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K000608 02/23/2000 SUCTION VASCULAR STAPLER AND IMPLANTABLE STAPLE SYSTEM STD MFG., INC.
K012362 07/25/2001 MODIFICATION TO VASCULAR CLOSURE DEVICE STD MFG., INC.
K003169 10/10/2000 VASCULAR CLOSURE DEVICE STD MFG., INC.
K021549 05/13/2002 CONTOURED ARTICULAR PROSTHESIS (CAP) FEMORAL HEAD RESURFACING SYSTEM STD MFG., INC.
K023096 09/18/2002 CONTOURED ARTICULAR PROSTHESIS (CAP) HUMERAL HEAD RESURFACING SYSTEM STD MFG., INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact