STRYKER 2S SPINAL SYSTEM
K-Number: K930009 · 1994-09-01
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Device Summary
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.
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
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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