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FDA 510(k)

BONE LAVAGE SYSTEM

K-Number: K926337 · 1993-06-11

ApplicantInnovative Surgical Devices Corp.
Decision Date1993-06-11
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BONE LAVAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Surgical Devices Corp.. It received FDA 510(k) clearance on 1993-06-11 under 510(k) number K926337. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE LAVAGE SYSTEM?

BONE LAVAGE SYSTEM is a medical device that received FDA 510(k) clearance on 1993-06-11. The listed applicant is Innovative Surgical Devices Corp.. The 510(k) number is K926337.

When did BONE LAVAGE SYSTEM receive FDA 510(k) clearance?

BONE LAVAGE SYSTEM received FDA 510(k) clearance on 1993-06-11, under 510(k) number K926337.

Who is the listed applicant for BONE LAVAGE SYSTEM?

The FDA 510(k) record lists Innovative Surgical Devices Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BONE LAVAGE SYSTEM?

The FDA product code for BONE LAVAGE SYSTEM is FQH.

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.

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Other records listing Innovative Surgical Devices Corp. 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.

K884404HERNIASTAT

Related Devices (Code: FQH)

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.

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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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