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ACUTE INNOVATIONS STERNAL FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101170
510(k) Type
Traditional
Applicant
ACUTE INNOVATIONS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2010
Days to Decision
144 days
Submission Type
Summary

ACUTE INNOVATIONS STERNAL FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101170
510(k) Type
Traditional
Applicant
ACUTE INNOVATIONS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2010
Days to Decision
144 days
Submission Type
Summary