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Release Laminoplasty Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153735
510(k) Type
Special
Applicant
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2016
Days to Decision
24 days
Submission Type
Summary

Release Laminoplasty Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153735
510(k) Type
Special
Applicant
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2016
Days to Decision
24 days
Submission Type
Summary