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
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K110734Substantially Equivalent

Nci Spatula

Fischer Surgical Inc., Imperial MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K110734 is the FDA 510(k) clearance record for NCI SPATULA, a class I device, cleared for Fischer Surgical, Inc. on under FDA product code OTZ (Graft Insertion Instrument For Endothelial Keratoplasty). FDA's definition for product code OTZ reads: "A graft insertion device for endothelial keratoplasty is a device intended to be inserted into the eye during surgery to direct the insertion of a corneal graft and be removed after insertion is completed". FDA records list one 510(k) clearance for Fischer Surgical, Inc. As of , FDA records show no recalls naming K110734.

Clearance record

Decision date
Received
(442 days to decision)
Product code
OTZ Graft Insertion Instrument For Endothelial Keratoplasty
Regulation
21 CFR 886.4300
Device class
Class I
Review panel
Ophthalmic
Applicant
Fischer Surgical, Inc. 1012 Palmer Ln.,, Imperial MO
510(k) summary
Statement
Third party review
No

Clearances, product code OTZ

Trailing 12 months

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

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