MODULOCK POSTERIOR SPINAL FIXATION
K-Number: K902397 · 1990-11-05
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Device Summary
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.
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
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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