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FDA 510(k)

TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE)

K-Number: K003911 · 2001-03-13

ApplicantTerray Corp.
Decision Date2001-03-13
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE) is the device name listed in this FDA 510(k) record. The listed applicant is Terray Corp.. It received FDA 510(k) clearance on 2001-03-13 under 510(k) number K003911. 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 TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE)?

TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE) is a medical device that received FDA 510(k) clearance on 2001-03-13. The listed applicant is Terray Corp.. The 510(k) number is K003911.

When did TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE) receive FDA 510(k) clearance?

TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE) received FDA 510(k) clearance on 2001-03-13, under 510(k) number K003911.

Who is the listed applicant for TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE)?

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

What is the FDA product code for TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE)?

The FDA product code for TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE) is KWP.

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Other records listing Terray Corp. 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.

K063275DISTAL CLAVICULAR FRAGMENT IMMOBILIZATION PLATE LEFT, MODEL 1810-116_126-03 (05,07) RIGHT 1811-116_126-03 (05,07)K003629MTP RESESURFACING JOINT-SMALL/9301-01; MEDIUM/9301-02; LARGE/9301-03K974030CARPAL ENGAGING WRIST FUSION PLATE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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