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APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102820
510(k) Type
Traditional
Applicant
ALPHATEC SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2010
Days to Decision
38 days
Submission Type
Summary

APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102820
510(k) Type
Traditional
Applicant
ALPHATEC SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2010
Days to Decision
38 days
Submission Type
Summary