510(k) K870729
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