Last synced on 18 April 2025 at 11:05 pm

SYNTHES DORSAL DISTAL RADIUS PLATE (DDRP) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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