Last synced on 18 April 2025 at 11:05 pm

BONE-LOCK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954030
510(k) Type
Traditional
Applicant
LEIBINGER GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1997
Days to Decision
809 days
Submission Type
Summary

BONE-LOCK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954030
510(k) Type
Traditional
Applicant
LEIBINGER GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1997
Days to Decision
809 days
Submission Type
Summary