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FDA 510(k)

HOPPENSTEIN MICROSURGICAL SPINAL INSTRU

K-Number: K842701 · 1984-08-02

ApplicantDowns Surgical , Ltd.
Decision Date1984-08-02
Product CodeFZS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOPPENSTEIN MICROSURGICAL SPINAL INSTRU is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1984-08-02 under 510(k) number K842701. The device is classified under product code FZS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOPPENSTEIN MICROSURGICAL SPINAL INSTRU?

HOPPENSTEIN MICROSURGICAL SPINAL INSTRU is a medical device that received FDA 510(k) clearance on 1984-08-02. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K842701.

When did HOPPENSTEIN MICROSURGICAL SPINAL INSTRU receive FDA 510(k) clearance?

HOPPENSTEIN MICROSURGICAL SPINAL INSTRU received FDA 510(k) clearance on 1984-08-02, under 510(k) number K842701.

Who is the listed applicant for HOPPENSTEIN MICROSURGICAL SPINAL INSTRU?

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

What is the FDA product code for HOPPENSTEIN MICROSURGICAL SPINAL INSTRU?

The FDA product code for HOPPENSTEIN MICROSURGICAL SPINAL INSTRU is FZS.

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Related Devices (Code: FZS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K932493SURGICAL CURETTEWhitney Products, Inc.K902000KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELDKevtek Medical Products, Inc.K892521CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVECymed, Inc.K891888CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPERZinnanti Surgical Instruments, Inc.K891334ACU-CURETTEAcuderm, Inc.K890366ADENOID CURETTEKinetic Medical Products

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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