DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM
K-Number: K980368 · 1998-04-14
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Device Summary
Frequently Asked Questions
What is the DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM?
DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM is a medical device that received FDA 510(k) clearance on 1998-04-14. The listed applicant is Depuy, Inc.. The 510(k) number is K980368.
When did DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM receive FDA 510(k) clearance?
DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM received FDA 510(k) clearance on 1998-04-14, under 510(k) number K980368.
Who is the listed applicant for DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM?
The FDA 510(k) record lists Depuy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM?
The FDA product code for DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM is HRS.
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 Depuy, 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: HRS)
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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