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BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080761
510(k) Type
Traditional
Applicant
Bonart Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2008
Days to Decision
160 days
Submission Type
Statement

BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080761
510(k) Type
Traditional
Applicant
Bonart Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2008
Days to Decision
160 days
Submission Type
Statement