GUIDE WIRES FOR CANNULATED SCREWS— 510(k) K963432
Substantially EquivalentOrthopaedic Biosystems, Ltd.
FDA 510(k) clearance K963432 for GUIDE WIRES FOR CANNULATED SCREWS, Substantially Equivalent on 1996-11-13. Applicant: Orthopaedic Biosystems, Ltd.. Device class: 2.
Clearance details
- Applicant
- Orthopaedic Biosystems, Ltd.
- Product code
- Code LXT
- Device class
- Class 2
- Regulation
- 21 CFR 888.3030
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Scotsdale, AZ, US
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