Last synced on 14 November 2025 at 11:06 pm

MAXLOCK EXTREME SYSTEM MODEL MXL

Page Type
Cleared 510(K)
510(k) Number
K123203
510(k) Type
Traditional
Applicant
ORTHOHELIX SURGICAL DESIGNS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2012
Days to Decision
63 days
Submission Type
Summary

MAXLOCK EXTREME SYSTEM MODEL MXL

Page Type
Cleared 510(K)
510(k) Number
K123203
510(k) Type
Traditional
Applicant
ORTHOHELIX SURGICAL DESIGNS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2012
Days to Decision
63 days
Submission Type
Summary