RESURFACE PROSHESIS— 510(k) K781343
Substantially EquivalentAesculap Instruments Corp.
FDA 510(k) clearance K781343 for RESURFACE PROSHESIS, Substantially Equivalent on 1978-09-27. Applicant: Aesculap Instruments Corp..
Clearance details
- Applicant
- Aesculap Instruments Corp.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.