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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Saw, Pneumatically Powered
510(k) Number K870157
Device Name OSCILLATING SAW/ RECIPROCATING SAW/ DRILL-REAMER
Applicant
Micro-Aire Surgical Instruments, Inc.
505 Fourth St.
San Fernando,  CA  91340
Applicant Contact SIDDHARTH DESAI
Correspondent
Micro-Aire Surgical Instruments, Inc.
505 Fourth St.
San Fernando,  CA  91340
Correspondent Contact SIDDHARTH DESAI
Regulation Number878.4820
Classification Product Code
KFK  
Date Received01/13/1987
Decision Date 02/24/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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