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FDA 510(k)

STRYKER INJECTABLE CEMENT

K-Number: K060750 · 2006-04-19

ApplicantStryker Cmf
Decision Date2006-04-19
Product CodeNEA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STRYKER INJECTABLE CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Cmf. It received FDA 510(k) clearance on 2006-04-19 under 510(k) number K060750. The device is classified under product code NEA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER INJECTABLE CEMENT?

STRYKER INJECTABLE CEMENT is a medical device that received FDA 510(k) clearance on 2006-04-19. The listed applicant is Stryker Cmf. The 510(k) number is K060750.

When did STRYKER INJECTABLE CEMENT receive FDA 510(k) clearance?

STRYKER INJECTABLE CEMENT received FDA 510(k) clearance on 2006-04-19, under 510(k) number K060750.

Who is the listed applicant for STRYKER INJECTABLE CEMENT?

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

What is the FDA product code for STRYKER INJECTABLE CEMENT?

The FDA product code for STRYKER INJECTABLE CEMENT is NEA.

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.

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Other records listing Stryker Cmf 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.

K071628STRYKER EXTERNAL FIXATION SYSTEM

Related Devices (Code: NEA)

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.

K080032ENVOYCEM, MODEL 1640Envoy Medical CorporationK042516OTOMIMIXWalter Lorenz Surgical, Inc.K011338OTO-CEMOtotech, Inc.K003567SERENOCEM, MODEL BC 010Corinthian Medical , Ltd.

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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