510(k) K960807

TEW CRANIAL/SPINAL RETRACTOR MODEL A1090 by Ohio Medical Instrument Co., Inc. — Product Code GZT

K960807 is an FDA 510(k) premarket notification submitted by Ohio Medical Instrument Co., Inc. for the device "TEW CRANIAL/SPINAL RETRACTOR MODEL A1090". The FDA issued a decision of Substantially Equivalent on May 17, 1996. The device falls under product code GZT (Retractor, Self-Retaining, For Neurosurgery), a Class II device regulated under 21 CFR 882.4800. Ohio Medical Instrument Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 17, 1996
Date Received
February 28, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Retractor, Self-Retaining, For Neurosurgery
Device Class
Class II
Regulation Number
882.4800
Review Panel
NE
Submission Type