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FDA 510(k)

HENNING MENISCAL SUTURE KIT

K-Number: K843942 · 1985-04-15

ApplicantStryker Corp.
Decision Date1985-04-15
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HENNING MENISCAL SUTURE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1985-04-15 under 510(k) number K843942. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HENNING MENISCAL SUTURE KIT?

HENNING MENISCAL SUTURE KIT is a medical device that received FDA 510(k) clearance on 1985-04-15. The listed applicant is Stryker Corp.. The 510(k) number is K843942.

When did HENNING MENISCAL SUTURE KIT receive FDA 510(k) clearance?

HENNING MENISCAL SUTURE KIT received FDA 510(k) clearance on 1985-04-15, under 510(k) number K843942.

Who is the listed applicant for HENNING MENISCAL SUTURE KIT?

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

What is the FDA product code for HENNING MENISCAL SUTURE KIT?

The FDA product code for HENNING MENISCAL SUTURE KIT is LXH.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: LXH)

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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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