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FDA 510(k)

ACROMED SPINAL SURGERY INSTRUMENTS

K-Number: K860131 · 1986-03-19

Decision Date1986-03-19
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED SPINAL SURGERY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1986-03-19 under 510(k) number K860131. 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 ACROMED SPINAL SURGERY INSTRUMENTS?

ACROMED SPINAL SURGERY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1986-03-19. The listed applicant is Buckman Co., Inc.. The 510(k) number is K860131.

When did ACROMED SPINAL SURGERY INSTRUMENTS receive FDA 510(k) clearance?

ACROMED SPINAL SURGERY INSTRUMENTS received FDA 510(k) clearance on 1986-03-19, under 510(k) number K860131.

Who is the listed applicant for ACROMED SPINAL SURGERY INSTRUMENTS?

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

What is the FDA product code for ACROMED SPINAL SURGERY INSTRUMENTS?

The FDA product code for ACROMED SPINAL SURGERY INSTRUMENTS is LXH.

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 Buckman Co., 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 111 devices →

Related Devices (Code: LXH)

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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