ACROMED SPINAL SURGERY INSTRUMENTS
K-Number: K860131 · 1986-03-19
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Device Summary
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.
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
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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