FLUTED SUCTION MENISCAL CUTTER— 510(k) K850789

Name: FDA 510(k) clearance K850789
Creator: U.S. Food and Drug Administration
Published: 1985-06-28

Substantially Equivalent

T. Korossurgical Instruments Corp.

FDA 510(k) clearance K850789 for FLUTED SUCTION MENISCAL CUTTER, Substantially Equivalent on 1985-06-28. Applicant: T. Korossurgical Instruments Corp.. Device class: 1.

Clearance details

Applicant: T. Korossurgical Instruments Corp.
Product code: Code KIJ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1985-02-26
Decision date: 1985-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westlake, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIJ

view all

K163308 — SMARTO2016-12-27
K112599 — INSURGICAL SINGLE USE POWER EQUIPMENT2012-11-06
K101563 — SMARTO2010-12-17
K972367 — STRYKER SYSTEM 4000 HEAVY DUTY BATTERY POWERED EQUIPMENT1997-09-04
K970378 — STRYKER 2115 REPLACEMENT BATTERY (2115)1997-04-30

More clearances from T. Korossurgical Instruments Corp.

view all

K001915 — GRAFT MARKER RING2001-04-27
K002755 — NON-ABSORBING STERNATOMY MONOFILAMENT SUTURE2000-12-04
K954016 — VIDEOSCOPE W/IRRIGATION SHEATH1996-01-25
K953998 — DISCETOME TISSUE ASPIRATOR1995-12-04
K954014 — PERCUTANEOUS DISCECTOMY CANNULA SYSTEM1995-11-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.