FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SIMEX SUCTION PUMP, MODELS AC20, AC20K, AC30, DC20, DC30 AND DC30S

K Number: K061133 · Decision Jul 11, 2006
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
3
Review Days
78

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Basic Information

Device Name
SIMEX SUCTION PUMP, MODELS AC20, AC20K, AC30, DC20, DC30 AND DC30S
K Number
K061133
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Novaspine, LLC
Date Received
April 24, 2006
Decision Date
July 11, 2006
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

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Other Clearances by Novaspine, LLC

K Number Device Name
K062456 NOVASPINE POWERED SUCTION PUMP PRO-1
K051607 NOVASPINE CEMENT RESTRICTOR NSCR