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KANGLI PEDICLE SCREW SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140053
510(k) Type
Traditional
Applicant
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/26/2014
Days to Decision
168 days
Submission Type
Summary

KANGLI PEDICLE SCREW SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140053
510(k) Type
Traditional
Applicant
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/26/2014
Days to Decision
168 days
Submission Type
Summary