510(k) K830332

BUDDE-HALO RETRACTOR by Ohio Medical Instrument Co., Inc. — Product Code GZT

K830332 is an FDA 510(k) premarket notification submitted by Ohio Medical Instrument Co., Inc. for the device "BUDDE-HALO RETRACTOR". The FDA issued a decision of Substantially Equivalent on March 2, 1983. 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
March 2, 1983
Date Received
February 1, 1983
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