Last synced on 20 December 2024 at 11:05 pm

LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993990
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2000
Days to Decision
90 days
Submission Type
Summary

LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993990
510(k) Type
Traditional
Applicant
STRYKER INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2000
Days to Decision
90 days
Submission Type
Summary