PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS
K-Number: K924381 · 1993-05-18
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Device Summary
Frequently Asked Questions
What is the PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS?
PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS is a medical device that received FDA 510(k) clearance on 1993-05-18. The listed applicant is Cross Medical Products, Inc.. The 510(k) number is K924381.
When did PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS receive FDA 510(k) clearance?
PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS received FDA 510(k) clearance on 1993-05-18, under 510(k) number K924381.
Who is the listed applicant for PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS?
The FDA 510(k) record lists Cross Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS?
The FDA product code for PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS 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 Cross Medical Products, 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.
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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