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SP-Fix® Spinous Process Fixation Plate, RELIEVE® Laminoplasty Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180156
510(k) Type
Traditional
Applicant
Globus Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2018
Days to Decision
47 days
Submission Type
Summary

SP-Fix® Spinous Process Fixation Plate, RELIEVE® Laminoplasty Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180156
510(k) Type
Traditional
Applicant
Globus Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2018
Days to Decision
47 days
Submission Type
Summary