DEPUY ACE SPIDER PLATE
K-Number: K984458 · 1998-12-31
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Device Summary
Frequently Asked Questions
What is the DEPUY ACE SPIDER PLATE?
DEPUY ACE SPIDER PLATE is a medical device that received FDA 510(k) clearance on 1998-12-31. The listed applicant is Depuy Ace Medical Co.. The 510(k) number is K984458.
When did DEPUY ACE SPIDER PLATE receive FDA 510(k) clearance?
DEPUY ACE SPIDER PLATE received FDA 510(k) clearance on 1998-12-31, under 510(k) number K984458.
Who is the listed applicant for DEPUY ACE SPIDER PLATE?
The FDA 510(k) record lists Depuy Ace Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEPUY ACE SPIDER PLATE?
The FDA product code for DEPUY ACE SPIDER PLATE 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 Ace Medical Co. 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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