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FDA 510(k)

STRYKER 2S SPINAL SYSTEM

K-Number: K930009 · 1994-09-01

ApplicantStryker Corp.
Decision Date1994-09-01
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER 2S SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1994-09-01 under 510(k) number K930009. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER 2S SPINAL SYSTEM?

STRYKER 2S SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 1994-09-01. The listed applicant is Stryker Corp.. The 510(k) number is K930009.

When did STRYKER 2S SPINAL SYSTEM receive FDA 510(k) clearance?

STRYKER 2S SPINAL SYSTEM received FDA 510(k) clearance on 1994-09-01, under 510(k) number K930009.

Who is the listed applicant for STRYKER 2S SPINAL SYSTEM?

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 STRYKER 2S SPINAL SYSTEM?

The FDA product code for STRYKER 2S SPINAL SYSTEM is KWP.

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 Stryker 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.

View all 119 devices →

Related Devices (Code: KWP)

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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