510(k) K905383

2710-000 OSCILLATING SAW, GENERAL ASSEMBLY by Micro Surgical Instruments Corp. — Product Code GEY

K905383 is an FDA 510(k) premarket notification submitted by Micro Surgical Instruments Corp. for the device "2710-000 OSCILLATING SAW, GENERAL ASSEMBLY". The FDA issued a decision of Substantially Equivalent on June 18, 1991. The device falls under product code GEY (Motor, Surgical Instrument, Ac-Powered), a Class I device regulated under 21 CFR 878.4820. Micro Surgical Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 18, 1991
Date Received
November 29, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Motor, Surgical Instrument, Ac-Powered
Device Class
Class I
Regulation Number
878.4820
Review Panel
SU
Submission Type