Last synced on 23 May 2025 at 11:06 pm

HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961511
510(k) Type
Traditional
Applicant
LIFECORE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1996
Days to Decision
70 days
Submission Type
Summary

HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961511
510(k) Type
Traditional
Applicant
LIFECORE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1996
Days to Decision
70 days
Submission Type
Summary