510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802524Substantially Equivalent

Surgical Hammers

Midshore Welding Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802524 is the FDA 510(k) clearance record for SURGICAL HAMMERS, a class I device, cleared for Midshore Welding Corp. on under FDA product code FZY (Hammer, Surgical). FDA records list one 510(k) clearance for Midshore Welding Corp. As of , FDA records show no recalls naming K802524.

Clearance record

Decision date
Received
(27 days to decision)
Product code
FZY Hammer, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Midshore Welding Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FZY

Trailing 12 months

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

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