LAURE WRIST IMPLANT— 510(k) K803031

Substantially Equivalent

Laure Prosthetics, Inc.

FDA 510(k) clearance K803031 for LAURE WRIST IMPLANT, Substantially Equivalent on 1982-06-29. Applicant: Laure Prosthetics, Inc..

Clearance details

Applicant
Laure Prosthetics, Inc.
Product code
Code KWM
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.