510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002755Substantially Equivalent

Non-Absorbing Sternatomy Monofilament Suture

T. Korossurgical Instruments Corp., Moorepark CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002755 is the FDA 510(k) clearance record for NON-ABSORBING STERNATOMY MONOFILAMENT SUTURE, a class II device, cleared for T. Korossurgical Instruments Corp. on under FDA product code LRN (Wire, Surgical). FDA records list 27 510(k) clearances for T. Korossurgical Instruments Corp., from to . As of , FDA records show no recalls naming K002755.

Clearance record

Decision date
Received
(90 days to decision)
Product code
LRN Wire, Surgical
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
T. Korossurgical Instruments Corp. 610 Flinn Ave., Moorepark CA
510(k) summary
Statement
Third party review
No

Clearances, product code LRN

Trailing 12 months

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

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