CERAVITAL CERAMIC OSSICULAR REPL. PROS.— 510(k) K810707
Substantially EquivalentXomed, Inc.
FDA 510(k) clearance K810707 for CERAVITAL CERAMIC OSSICULAR REPL. PROS., Substantially Equivalent on 1981-06-16. Applicant: Xomed, Inc.. Device class: 2.
Clearance details
- Applicant
- Xomed, Inc.
- 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
- Arnold, MO, US
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More clearances from Xomed, Inc.
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