P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG— 510(k) K863854
Substantially EquivalentPrecision Medical Devices, Inc.
FDA 510(k) clearance K863854 for P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG, Substantially Equivalent on 1986-11-19. Applicant: Precision Medical Devices, Inc..
Clearance details
- Applicant
- Precision Medical Devices, Inc.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Camp Hill, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.