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FDA 510(k)

DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS

K-Number: K983583 · 1998-12-03

ApplicantDepuy, Inc.
Decision Date1998-12-03
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1998-12-03 under 510(k) number K983583. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS?

DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS is a medical device that received FDA 510(k) clearance on 1998-12-03. The listed applicant is Depuy, Inc.. The 510(k) number is K983583.

When did DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS receive FDA 510(k) clearance?

DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS received FDA 510(k) clearance on 1998-12-03, under 510(k) number K983583.

Who is the listed applicant for DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS?

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 ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS?

The FDA product code for DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS is KWP.

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Other records listing Depuy, Inc. as applicant

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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.

K133094CERTEX OCT SPINAL IMPLANT SYSTEMX-Spine Systems, Inc.K132504TIGER OCCIPITAL-CERVICAL-THORACIC SPINAL FIXATION SYSTEMCorelink, LLCK132900MARAUDER CERVICAL-THORACIC SPINAL FIXATION SYSTEMIntelligent Implant Systems, LLCK131427LOTUSSpinal Elements, Inc.K132332MOUNTAINEER OCT SPINAL SYSTEMMedos International SARLK131156LANX SPINAL FIXATION SYSTEMLanx, Inc.

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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