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MENNEN BONE FIXATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892411
510(k) Type
Traditional
Applicant
DENTSPLY INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1990
Days to Decision
273 days

MENNEN BONE FIXATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892411
510(k) Type
Traditional
Applicant
DENTSPLY INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1990
Days to Decision
273 days