Micra Microsurgical Instruments

FDA 510(k) K862971 · Cordis Corp.

Substantially Equivalent

510(k) numberK862971

Submission

Device name
Micra Microsurgical Instruments
Applicant
Cordis Corp.
Miami, FL, US
Received
August 6, 1986
Decision date
August 25, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GZX – Instrument, Microsurgical
Device class
Class I (low risk)
Regulation
21 CFR 882.4525
Specialty
Neurology

Other 510(k)s with product code GZX

510(k)DeviceApplicantDecision
K932169Microsurgical InstrumentsGZX · Traditional American Russian Medical Services, Inc.07/20/1993SE
K926048Clarus Endoscopic Ball ProbeGZX · Traditional Clarus Medical Systems, Inc.04/07/1993SE
K911932J105 James Surgical System I/A PackGZX · Traditional O.R. Specialties, Inc.08/26/1991SE
K890216Microsurgical KeratomeGZX · Traditional Kinetic Medical Products02/16/1989SE
K873934Range of Crocodile Action InstrumentsGZX · Traditional Downs Surgical , Ltd.12/17/1987SE
K873933Range of Neurosurgical Instruments in TitaniumGZX · Traditional Downs Surgical , Ltd.12/17/1987SE
K853179Vickers Ergomatic Microsur Instru-Univ R O L HandGZX · Traditional Keeler Instruments, Inc.11/07/1985SE
K853161The Vickers Standard Microsurgery SetGZX · Traditional Keeler Instruments, Inc.11/07/1985SE
K853181Vickers Ergomatic Micros Instr-Fine R or L HandedGZX · Traditional Keeler Instruments, Inc.10/28/1985SE
K853180Vickers Ergomatic Micros Instr-Long R or L HandedGZX · Traditional Keeler Instruments, Inc.10/28/1985SE

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Questions and answers

When was Micra Microsurgical Instruments cleared by the FDA?

Micra Microsurgical Instruments (K862971) received a 510(k) decision of Substantially Equivalent on August 25, 1986, 19 days after the submission was received.

What is the product code of K862971?

The FDA product code is GZX – Instrument, Microsurgical, a Class I (low risk) device regulated under 21 CFR 882.4525.