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PARAGON POSTERIOR SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920546
510(k) Type
Traditional
Applicant
SOFAMOR DANEK MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/21/1993
Days to Decision
350 days
Submission Type
Statement

PARAGON POSTERIOR SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920546
510(k) Type
Traditional
Applicant
SOFAMOR DANEK MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/21/1993
Days to Decision
350 days
Submission Type
Statement