CAUSSE UNIVERSAL OSSICULAR REPLACEMENT PROSTHESIS (ORP/1)— 510(k) K963899
Substantially EquivalentExmoor Plastics , Ltd.
FDA 510(k) clearance K963899 for CAUSSE UNIVERSAL OSSICULAR REPLACEMENT PROSTHESIS (ORP/1), Substantially Equivalent on 1997-08-22. Applicant: Exmoor Plastics , Ltd..
Clearance details
- Applicant
- Exmoor Plastics , Ltd.
- Product code
- Code ETA
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Taunton, GB
Data sourced from openFDA. This site is unofficial and independent of the FDA.