MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE— 510(k) K915139

Name: FDA 510(k) clearance K915139
Creator: U.S. Food and Drug Administration
Published: 1992-02-05

Substantially Equivalent

Micro Surgical Instruments Corp.

FDA 510(k) clearance K915139 for MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE, Substantially Equivalent on 1992-02-05. Applicant: Micro Surgical Instruments Corp.. Device class: 1.

Clearance details

Applicant: Micro Surgical Instruments Corp.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1991-11-13
Decision date: 1992-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HSZ

view all

K991588 — EMS SWISS ORTHOCLAST1999-07-21
K972860 — CURVTEK TSR SYSTEM1997-10-31
K970345 — ALIGNMENT INSTRUMENT1997-04-29
K955084 — ASPACH 65,000 (MODIFICATION)1996-01-17
K954080 — SODEM HIGH SPEED SYSTEM1995-10-16

More clearances from Micro Surgical Instruments Corp.

view all

K931395 — SERIES 5000 BATTERY POWERED INSTRUMENT SYSTEM1994-01-28
K932492 — IMPLANTOLOGY MODULE, MODEL 21751993-10-05
K930205 — ELECTRIC WIRE DRIVER, MODEL 2640E1993-08-02
K914998 — MICROAIRE(R) FACIAL BONE PLATING SYSTEM1992-06-02
K914346 — DRILL MODULES MODELS 2116/21171991-11-27

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