OSTEOMARK— 510(k) K980518

Substantially Equivalent

Ostex Intl., Inc.

FDA 510(k) clearance K980518 for OSTEOMARK, Substantially Equivalent on 1998-03-06. Applicant: Ostex Intl., Inc..

Clearance details

Applicant: Ostex Intl., Inc.
Product code: Code JMM
Advisory panel: Clinical Chemistry
Date received: 1998-01-16
Decision date: 1998-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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