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/ Piezosurgery S.R.L.
Piezosurgery S.R.L.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
5
Compliance Actions
1
Recent 510(k) Clearances
K-Number
Device
Date
K091227
PIEZOSURGERY 3; OSSTEM PIEZO
December 29, 2009
K083284
PIEZOSURGERY MEDICAL
April 8, 2009
K052518
PIEZOSURGERY
November 16, 2005
K043408
PIEZOSURGERY DEVICE
June 8, 2005