Last synced on 14 November 2025 at 11:06 pm

BIOBOLT

Page Type
Cleared 510(K)
510(k) Number
K120540
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2012
Days to Decision
26 days
Submission Type
Summary

BIOBOLT

Page Type
Cleared 510(K)
510(k) Number
K120540
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2012
Days to Decision
26 days
Submission Type
Summary