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FDA 510(k)

CONTOUR SPINAL SYSTEM

K-Number: K990986 · 1999-10-14

ApplicantOrtho Development Corp.
Decision Date1999-10-14
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONTOUR SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Development Corp.. It received FDA 510(k) clearance on 1999-10-14 under 510(k) number K990986. 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 CONTOUR SPINAL SYSTEM?

CONTOUR SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 1999-10-14. The listed applicant is Ortho Development Corp.. The 510(k) number is K990986.

When did CONTOUR SPINAL SYSTEM receive FDA 510(k) clearance?

CONTOUR SPINAL SYSTEM received FDA 510(k) clearance on 1999-10-14, under 510(k) number K990986.

Who is the listed applicant for CONTOUR SPINAL SYSTEM?

The FDA 510(k) record lists Ortho Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTOUR SPINAL SYSTEM?

The FDA product code for CONTOUR SPINAL SYSTEM is KWP.

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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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