Last synced on 30 May 2025 at 11:05 pm

MODULAR THUMB IMPLANT, MODELS 17065,17066,17243,17067,17199,17238,17005,17239,17006,17240,17007,17241,17500,17501,17507

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052596
510(k) Type
Traditional
Applicant
BIOPRO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2005
Days to Decision
55 days
Submission Type
Summary

MODULAR THUMB IMPLANT, MODELS 17065,17066,17243,17067,17199,17238,17005,17239,17006,17240,17007,17241,17500,17501,17507

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052596
510(k) Type
Traditional
Applicant
BIOPRO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2005
Days to Decision
55 days
Submission Type
Summary