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ARTHROSTEER ABLATOR & COAGULATOR, MODELS: REF 1070 & 1080

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093086
510(k) Type
Traditional
Applicant
ORTHODYNAMIX, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2010
Days to Decision
145 days
Submission Type
Statement

ARTHROSTEER ABLATOR & COAGULATOR, MODELS: REF 1070 & 1080

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093086
510(k) Type
Traditional
Applicant
ORTHODYNAMIX, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2010
Days to Decision
145 days
Submission Type
Statement