510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K870729Substantially Equivalent

Titanium Percutaneous Greenfield Vena Cave Filter

Medi-Tech, Inc., Watertown MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870729 is the FDA 510(k) clearance record for TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER, a class II device, cleared for Medi-Tech, Inc. on under FDA product code DTK (Filter, Intravascular, Cardiovascular). FDA records list 36 510(k) clearances for Medi-Tech, Inc., from to . As of , FDA records show no recalls naming K870729.

Clearance record

Decision date
Received
(43 days to decision)
Product code
DTK Filter, Intravascular, Cardiovascular
Regulation
21 CFR 870.3375
Device class
Class II
Review panel
Cardiovascular
Applicant
Medi-Tech, Inc. 480 Plesant St., Watertown MA
Third party review
No

Clearances, product code DTK

Trailing 12 months

FDA records hold no clearances under product code DTK in the trailing twelve months.

FDA records show no clearances under product code DTK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DTK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260