ZURICH TITANIUM OSSICULAR REPLACEMENT SYSTEM— 510(k) K993583
Substantially EquivalentStryker Corp.
FDA 510(k) clearance K993583 for ZURICH TITANIUM OSSICULAR REPLACEMENT SYSTEM, Substantially Equivalent on 1999-11-10. Applicant: Stryker Corp.. Device class: 2.
Clearance details
- Applicant
- Stryker Corp.
- Product code
- Code ETA
- Device class
- Class 2
- Regulation
- 21 CFR 874.3495
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kalamazoo, MI, US
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More clearances from Stryker Corp.
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