510(k) K042734

SJM RIGID SADDLE RING MODEL RSAR-(SIZE) by St. Jude Medical, Inc. — Product Code KRH

K042734 is an FDA 510(k) premarket notification submitted by St. Jude Medical, Inc. for the device "SJM RIGID SADDLE RING MODEL RSAR-(SIZE)". The FDA issued a decision of Substantially Equivalent on December 17, 2004. The device falls under product code KRH (Ring, Annuloplasty), a Class II device regulated under 21 CFR 870.3800. St. Jude Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 17, 2004
Date Received
October 1, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ring, Annuloplasty
Device Class
Class II
Regulation Number
870.3800
Review Panel
CV
Submission Type