Last synced on 30 May 2025 at 11:05 pm

MODULAR THUMB IMPLANT, MODELS 17600, 17601, 17602, 17603, 17596, 17597, 17598, 17599

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061089
510(k) Type
Traditional
Applicant
BIOPRO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2006
Days to Decision
63 days
Submission Type
Statement

MODULAR THUMB IMPLANT, MODELS 17600, 17601, 17602, 17603, 17596, 17597, 17598, 17599

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061089
510(k) Type
Traditional
Applicant
BIOPRO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2006
Days to Decision
63 days
Submission Type
Statement