Last synced on 14 November 2025 at 11:06 pm

BONE-LOCK

Page Type
Cleared 510(K)
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)
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