510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K220920Substantially Equivalent

Matreneu Percutaneous Balloon Compression Kit

Shenzhen Shineyard Medical Device Co., Ltd., Shenzhen, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K220920 is the FDA 510(k) clearance record for Matreneu Percutaneous Balloon Compression Kit, a class I device, cleared for Shenzhen Shineyard Medical Device Co. , Ltd. on under FDA product code HAO (Instrument, Surgical, Non-Powered). FDA records list one 510(k) clearance for Shenzhen Shineyard Medical Device Co. , Ltd. As of , FDA records show no recalls naming K220920.

Clearance record

Decision date
Received
(161 days to decision)
Product code
HAO Instrument, Surgical, Non-Powered
Regulation
21 CFR 882.4535
Device class
Class I
Review panel
Neurology
Applicant
Shenzhen Shineyard Medical Device Co. , Ltd. 3f, Changfeng Industrial Block #3 Liuxian Rd.,, Shenzhen, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HAO

Trailing 12 months

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

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