510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K060973Substantially Equivalent

Vycor Surgical Access Systems

Vycor Medical, Inc., Shelton CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060973 is the FDA 510(k) clearance record for VYCOR SURGICAL ACCESS SYSTEMS, a class II device, cleared for Vycor Medical, LLC on under FDA product code GZT (Retractor, Self-Retaining, For Neurosurgery). FDA records list 2 510(k) clearances for Vycor Medical, LLC, from to . As of , FDA records show one recall naming K060973.

Clearance record

Decision date
Received
(107 days to decision)
Product code
GZT Retractor, Self-Retaining, For Neurosurgery
Regulation
21 CFR 882.4800
Device class
Class II
Review panel
Neurology
Applicant
Vycor Medical, LLC 543 Long Hill Ave., Shelton CT
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code GZT

Trailing 12 months
1 clearance under product code GZT in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GZT, 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 20261
October 20260