Last synced on 23 May 2025 at 11:06 pm

SYNTHES SPINE POSTERIOR UNIVERSAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984612
510(k) Type
Special
Applicant
SYNTHES SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1999
Days to Decision
26 days
Submission Type
Summary

SYNTHES SPINE POSTERIOR UNIVERSAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984612
510(k) Type
Special
Applicant
SYNTHES SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1999
Days to Decision
26 days
Submission Type
Summary