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SPIDER SINGLE PORT SURGICAL DEVICE, SUPPORT ARM ACCESSORY, MODEL 90001, 90002, 90003

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090902
510(k) Type
Traditional
Applicant
TRANSENTERIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2009
Days to Decision
112 days
Submission Type
Summary