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FDA 510(k)

ACUMED PELVIC BONE PLATE SYSTEM

K-Number: K122538 · 2012-11-19

ApplicantAcumed, LLC
Decision Date2012-11-19
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACUMED PELVIC BONE PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Acumed, LLC. It received FDA 510(k) clearance on 2012-11-19 under 510(k) number K122538. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUMED PELVIC BONE PLATE SYSTEM?

ACUMED PELVIC BONE PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2012-11-19. The listed applicant is Acumed, LLC. The 510(k) number is K122538.

When did ACUMED PELVIC BONE PLATE SYSTEM receive FDA 510(k) clearance?

ACUMED PELVIC BONE PLATE SYSTEM received FDA 510(k) clearance on 2012-11-19, under 510(k) number K122538.

Who is the listed applicant for ACUMED PELVIC BONE PLATE SYSTEM?

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

What is the FDA product code for ACUMED PELVIC BONE PLATE SYSTEM?

The FDA product code for ACUMED PELVIC BONE PLATE SYSTEM is HRS.

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 Acumed, LLC 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.

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Related Devices (Code: HRS)

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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