510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K845035Substantially Equivalent for Some Indications

Electrode for Neurological Surgery 2111

Progress Mankind Technology, Hopkins MN / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K845035 is the FDA 510(k) clearance record for ELECTRODE FOR NEUROLOGICAL SURGERY 2111, a class II device, cleared for Progress Mankind Technology on under FDA product code GYC (Electrode, Cortical). FDA records list 17 510(k) clearances for Progress Mankind Technology, from to . As of , FDA records show no recalls naming K845035.

Clearance record

Decision date
Received
(215 days to decision)
Product code
GYC Electrode, Cortical
Regulation
21 CFR 882.1310
Device class
Class II
Review panel
Neurology
Applicant
Progress Mankind Technology Box 464, Hopkins MN
Third party review
No

Clearances, product code GYC

Trailing 12 months

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

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