510(k) K870729

TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER by Medi-Tech, Inc. — Product Code DTK

K870729 is an FDA 510(k) premarket notification submitted by Medi-Tech, Inc. for the device "TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER". The FDA issued a decision of Substantially Equivalent on April 9, 1987. The device falls under product code DTK (Filter, Intravascular, Cardiovascular), a Class II device regulated under 21 CFR 870.3375. Medi-Tech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 9, 1987
Date Received
February 25, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Intravascular, Cardiovascular
Device Class
Class II
Regulation Number
870.3375
Review Panel
CV
Submission Type