510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K970306Substantially Equivalent

Markman Template System

Barry Markman, M.D., Las Vegas NV / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970306 is the FDA 510(k) clearance record for MARKMAN TEMPLATE SYSTEM, a class I device, cleared for Barry Markman, M.D. on under FDA product code GAH (Stylet, Surgical, General & Plastic Surgery). FDA records list one 510(k) clearance for Barry Markman, M.D. As of , FDA records show no recalls naming K970306.

Clearance record

Decision date
Received
(297 days to decision)
Product code
GAH Stylet, Surgical, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Barry Markman, M.D. 3085 E. Flamingo, Suite A, Las Vegas NV
510(k) summary
Statement
Third party review
No

Clearances, product code GAH

Trailing 12 months

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

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