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FDA 510(k)

DEPUY SEGMENTALSPINAL SYSTEM

K-Number: K810329 · 1981-04-08

ApplicantDepuy, Inc.
Decision Date1981-04-08
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY SEGMENTALSPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1981-04-08 under 510(k) number K810329. 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 SEGMENTALSPINAL SYSTEM?

DEPUY SEGMENTALSPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 1981-04-08. The listed applicant is Depuy, Inc.. The 510(k) number is K810329.

When did DEPUY SEGMENTALSPINAL SYSTEM receive FDA 510(k) clearance?

DEPUY SEGMENTALSPINAL SYSTEM received FDA 510(k) clearance on 1981-04-08, under 510(k) number K810329.

Who is the listed applicant for DEPUY SEGMENTALSPINAL 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 SEGMENTALSPINAL SYSTEM?

The FDA product code for DEPUY SEGMENTALSPINAL SYSTEM is KWP.

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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.

K043058PINNACLE CONSTRAINED ACETABULAR LINERSK042664LPS UPPER EXTREMITYK041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARYK033959LPSK040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062K021478DELTA SHOULDER

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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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