510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K895369Substantially Equivalent

Voss Graft Marker

voss medical products, San Antonio TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895369 is the FDA 510(k) clearance record for VOSS GRAFT MARKER, a class II device, cleared for Voss Medical Products on under FDA product code KPK (Marker, Ostia, Aorto-Saphenous Vein). FDA records list 5 510(k) clearances for Voss Medical Products, from to . As of , FDA records show no recalls naming K895369.

Clearance record

Decision date
Received
(29 days to decision)
Product code
KPK Marker, Ostia, Aorto-Saphenous Vein
Regulation
21 CFR 878.4650
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Voss Medical Products 4227 Centergate, San Antonio TX
Third party review
No

Clearances, product code KPK

Trailing 12 months

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

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