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FDA 510(k)

MODULOCK POSTERIOR SPINAL FIXATION

K-Number: K902397 · 1990-11-05

ApplicantZimmer, Inc.
Decision Date1990-11-05
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

MODULOCK POSTERIOR SPINAL FIXATION is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1990-11-05 under 510(k) number K902397. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MODULOCK POSTERIOR SPINAL FIXATION?

MODULOCK POSTERIOR SPINAL FIXATION is a medical device that received FDA 510(k) clearance on 1990-11-05. The listed applicant is Zimmer, Inc.. The 510(k) number is K902397.

When did MODULOCK POSTERIOR SPINAL FIXATION receive FDA 510(k) clearance?

MODULOCK POSTERIOR SPINAL FIXATION received FDA 510(k) clearance on 1990-11-05, under 510(k) number K902397.

Who is the listed applicant for MODULOCK POSTERIOR SPINAL FIXATION?

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

What is the FDA product code for MODULOCK POSTERIOR SPINAL FIXATION?

The FDA product code for MODULOCK POSTERIOR SPINAL FIXATION 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 Zimmer, 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.

View all 344 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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