ORTHOREX INTRA-OPERATIVE LOAD SENSOR— 510(k) K090474
Substantially EquivalentOrthosensor, Inc.
FDA 510(k) clearance K090474 for ORTHOREX INTRA-OPERATIVE LOAD SENSOR, Substantially Equivalent on 2009-10-19. Applicant: Orthosensor, Inc.. Device class: 2.
Clearance details
- Applicant
- Orthosensor, Inc.
- Product code
- Code ONN
- Device class
- Class 2
- Regulation
- 21 CFR 882.4560
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Appollo Beach, FL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.