Last synced on 14 November 2025 at 11:06 pm

BONE WIRE

Page Type
Cleared 510(K)
510(k) Number
K030665
510(k) Type
Traditional
Applicant
STORK INSTRUMENTE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2003
Days to Decision
22 days
Submission Type
Summary

BONE WIRE

Page Type
Cleared 510(K)
510(k) Number
K030665
510(k) Type
Traditional
Applicant
STORK INSTRUMENTE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2003
Days to Decision
22 days
Submission Type
Summary