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FDA 510(k)

MEDNEXT 1000 BONE DISSECTING SYSTEM

K-Number: K926547 · 1993-07-22

ApplicantMednext, Inc.
Decision Date1993-07-22
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDNEXT 1000 BONE DISSECTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mednext, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K926547. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDNEXT 1000 BONE DISSECTING SYSTEM?

MEDNEXT 1000 BONE DISSECTING SYSTEM is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Mednext, Inc.. The 510(k) number is K926547.

When did MEDNEXT 1000 BONE DISSECTING SYSTEM receive FDA 510(k) clearance?

MEDNEXT 1000 BONE DISSECTING SYSTEM received FDA 510(k) clearance on 1993-07-22, under 510(k) number K926547.

Who is the listed applicant for MEDNEXT 1000 BONE DISSECTING SYSTEM?

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

What is the FDA product code for MEDNEXT 1000 BONE DISSECTING SYSTEM?

The FDA product code for MEDNEXT 1000 BONE DISSECTING SYSTEM is HSZ.

Related Clinical Trials

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.

Other records listing Mednext, Inc. as applicant

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.

View all 7 devices →

Related Devices (Code: HSZ)

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.

Official Source

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

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