TEW CRANIAL/SPINAL RETRACTOR MODEL A1090— 510(k) K960807
Substantially EquivalentOhio 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.. Device class: 2.
Clearance details
- Applicant
- Ohio Medical Instrument Co., Inc.
- Product code
- Code GZT
- Device class
- Class 2
- Regulation
- 21 CFR 882.4800
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cincinnati, OH, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.