510(k) K891203

SCISSORS: THOREK, JORGENSEN, FINOCHIETTO by Zinnanti Surgical Instruments, Inc. — Product Code LRW

K891203 is an FDA 510(k) premarket notification submitted by Zinnanti Surgical Instruments, Inc. for the device "SCISSORS: THOREK, JORGENSEN, FINOCHIETTO". The FDA issued a decision of Substantially Equivalent on April 6, 1989. The device falls under product code LRW (Scissors, General, Surgical), a Class I device regulated under 21 CFR 878.4800. Zinnanti Surgical Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 6, 1989
Date Received
March 6, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scissors, General, Surgical
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type