HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER— 510(k) K961511

Substantially Equivalent

Lifecore Biomedical, Inc.

FDA 510(k) clearance K961511 for HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER, Substantially Equivalent on 1996-06-28. Applicant: Lifecore Biomedical, Inc..

Clearance details

Applicant: Lifecore Biomedical, Inc.
Product code: Code LZK
Advisory panel: General, Plastic Surgery
Date received: 1996-04-19
Decision date: 1996-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chaska, MN, US

Download summary PDF View on FDA.gov ↗

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