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PMT SUBARACHNOID SCREW, MODEL NO.1350-2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883115
510(k) Type
Traditional
Applicant
PMT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1988
Days to Decision
35 days

PMT SUBARACHNOID SCREW, MODEL NO.1350-2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883115
510(k) Type
Traditional
Applicant
PMT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1988
Days to Decision
35 days