ACROMED SPINAL ROD AND SPINAL HOOKS
K-Number: K884163 · 1989-04-26
Advertisement
Device Summary
Frequently Asked Questions
What is the ACROMED SPINAL ROD AND SPINAL HOOKS?
ACROMED SPINAL ROD AND SPINAL HOOKS is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Buckman Co., Inc.. The 510(k) number is K884163.
When did ACROMED SPINAL ROD AND SPINAL HOOKS receive FDA 510(k) clearance?
ACROMED SPINAL ROD AND SPINAL HOOKS received FDA 510(k) clearance on 1989-04-26, under 510(k) number K884163.
Who is the listed applicant for ACROMED SPINAL ROD AND SPINAL HOOKS?
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 ROD AND SPINAL HOOKS?
The FDA product code for ACROMED SPINAL ROD AND SPINAL HOOKS 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 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: 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.
Advertisement