ACL DRILL GUIDE SYSTEM— 510(k) K892655
Substantially EquivalentBaxter Healthcare Corp
FDA 510(k) clearance K892655 for ACL DRILL GUIDE SYSTEM, Substantially Equivalent on 1989-09-28. Applicant: Baxter Healthcare Corp.
Clearance details
- Applicant
- Baxter Healthcare Corp
- Product code
- Code LXI
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Ana, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.