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FDA 510(k)

STRYKER PAINPUMP

K-Number: K014091 · 2001-12-31

ApplicantStryker Corp.
Decision Date2001-12-31
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER PAINPUMP is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2001-12-31 under 510(k) number K014091. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER PAINPUMP?

STRYKER PAINPUMP is a medical device that received FDA 510(k) clearance on 2001-12-31. The listed applicant is Stryker Corp.. The 510(k) number is K014091.

When did STRYKER PAINPUMP receive FDA 510(k) clearance?

STRYKER PAINPUMP received FDA 510(k) clearance on 2001-12-31, under 510(k) number K014091.

Who is the listed applicant for STRYKER PAINPUMP?

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

What is the FDA product code for STRYKER PAINPUMP?

The FDA product code for STRYKER PAINPUMP is FRN.

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Other records listing Stryker Corp. 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: FRN)

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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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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