TEW CRANIAL/SPINAL RETRACTOR MODEL A1090— 510(k) K960807

Substantially Equivalent

Ohio Medical Instrument Co., Inc.

FDA 510(k) clearance K960807 for TEW CRANIAL/SPINAL RETRACTOR MODEL A1090, Substantially Equivalent on 1996-05-17. Applicant: Ohio Medical Instrument Co., Inc..

Clearance details

Applicant: Ohio Medical Instrument Co., Inc.
Product code: Code GZT
Advisory panel: Neurology
Date received: 1996-02-28
Decision date: 1996-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

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