FDA 510(k)

ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator

Número K: K161065 · 2016-10-27

Data da decisão2016-10-27

Código do produtoHEW

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator is the device name listed in this FDA 510(k) record. The listed applicant is Surgitools Pty , Ltd.. It received FDA 510(k) clearance on 2016-10-27 under 510(k) number K161065. The device is classified under product code HEW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator?

ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator is a medical device that received FDA 510(k) clearance on 2016-10-27. The listed applicant is Surgitools Pty , Ltd.. The 510(k) number is K161065.

When did ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator receive FDA 510(k) clearance?

ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator received FDA 510(k) clearance on 2016-10-27, under 510(k) number K161065.

Who is the listed applicant for ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator?

The FDA 510(k) record lists Surgitools Pty , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator?

The FDA product code for ColpoWave™ Colpotomizer and CerviGrip™ Uterine Manipulator is HEW.

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