Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

POWER-LOAD COT FASTENER SYSTEM

K-Number: K113598 · 2011-12-20

Decision Date2011-12-20
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWER-LOAD COT FASTENER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Medical. It received FDA 510(k) clearance on 2011-12-20 under 510(k) number K113598. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER-LOAD COT FASTENER SYSTEM?

POWER-LOAD COT FASTENER SYSTEM is a medical device that received FDA 510(k) clearance on 2011-12-20. The listed applicant is Stryker Medical. The 510(k) number is K113598.

When did POWER-LOAD COT FASTENER SYSTEM receive FDA 510(k) clearance?

POWER-LOAD COT FASTENER SYSTEM received FDA 510(k) clearance on 2011-12-20, under 510(k) number K113598.

Who is the listed applicant for POWER-LOAD COT FASTENER SYSTEM?

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

What is the FDA product code for POWER-LOAD COT FASTENER SYSTEM?

The FDA product code for POWER-LOAD COT FASTENER SYSTEM is FPO.

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 Stryker Medical 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 14 devices →

Related Devices (Code: FPO)

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.

↑