510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071457Substantially Equivalent

Modification to Radius Snare

Radius Medical Technologies, Inc., Acton MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071457 is the FDA 510(k) clearance record for MODIFICATION TO RADIUS SNARE, a class II device, cleared for Radius Medical Technologies, Inc. on under FDA product code MMX (Device, Percutaneous Retrieval). FDA records list 9 510(k) clearances for Radius Medical Technologies, Inc., from to . As of , FDA records show no recalls naming K071457.

Clearance record

Decision date
Received
(123 days to decision)
Product code
MMX Device, Percutaneous Retrieval
Regulation
21 CFR 870.5150
Device class
Class II
Review panel
Cardiovascular
Applicant
Radius Medical Technologies, Inc. 15 Craig Rd., Acton MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MMX

Trailing 12 months

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

FDA records show no clearances under product code MMX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MMX, 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