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PIEZO BONE SURGERY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111290
510(k) Type
Traditional
Applicant
Guilin Woodpecker Medical Instrument Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2011
Days to Decision
196 days
Submission Type
Summary

PIEZO BONE SURGERY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111290
510(k) Type
Traditional
Applicant
Guilin Woodpecker Medical Instrument Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2011
Days to Decision
196 days
Submission Type
Summary