Last synced on 23 May 2025 at 11:06 pm

LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000594
510(k) Type
Traditional
Applicant
STRYKER LEIBINGER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2000
Days to Decision
290 days
Submission Type
Summary

LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000594
510(k) Type
Traditional
Applicant
STRYKER LEIBINGER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2000
Days to Decision
290 days
Submission Type
Summary