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SYNTHES DORSAL DISTAL RADIUS PLATE (DDRP) SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962616
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
9/3/1996
Days to Decision
62 days

SYNTHES DORSAL DISTAL RADIUS PLATE (DDRP) SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962616
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
9/3/1996
Days to Decision
62 days