510(k) K891398

RETRACTOR RODS by Zinnanti Surgical Instruments, Inc. — Product Code KNA

K891398 is an FDA 510(k) premarket notification submitted by Zinnanti Surgical Instruments, Inc. for the device "RETRACTOR RODS". The FDA issued a decision of Substantially Equivalent on May 11, 1989. The device falls under product code KNA (Instrument, Manual, Specialized Obstetric-Gynecologic), a Class II device regulated under 21 CFR 884.4530. Zinnanti Surgical Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 11, 1989
Date Received
March 14, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Manual, Specialized Obstetric-Gynecologic
Device Class
Class II
Regulation Number
884.4530
Review Panel
OB
Submission Type