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FDA 510(k)

ALPHA POSTERIOR SPINAL SYSTEM

K-Number: K964275 · 1997-01-14

Decision Date1997-01-14
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALPHA POSTERIOR SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sofamor Danek USA,Inc.. It received FDA 510(k) clearance on 1997-01-14 under 510(k) number K964275. 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 ALPHA POSTERIOR SPINAL SYSTEM?

ALPHA POSTERIOR SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 1997-01-14. The listed applicant is Sofamor Danek USA,Inc.. The 510(k) number is K964275.

When did ALPHA POSTERIOR SPINAL SYSTEM receive FDA 510(k) clearance?

ALPHA POSTERIOR SPINAL SYSTEM received FDA 510(k) clearance on 1997-01-14, under 510(k) number K964275.

Who is the listed applicant for ALPHA POSTERIOR SPINAL SYSTEM?

The FDA 510(k) record lists Sofamor Danek USA,Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALPHA POSTERIOR SPINAL SYSTEM?

The FDA product code for ALPHA POSTERIOR 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 Sofamor Danek USA,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.

View all 41 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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