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PIEZO ULTRASONIC DEVICE, MODEL ULTRASONIC BONE SURGERY; ULTRASONIC DEBRIDMENT DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080220
510(k) Type
Abbreviated
Applicant
Italia Medica S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2008
Days to Decision
181 days
Submission Type
Statement

PIEZO ULTRASONIC DEVICE, MODEL ULTRASONIC BONE SURGERY; ULTRASONIC DEBRIDMENT DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080220
510(k) Type
Abbreviated
Applicant
Italia Medica S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2008
Days to Decision
181 days
Submission Type
Statement