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FDA 510(k)

CTI STRAIGHT STEM

K-Number: K873627 · 1987-12-30

ApplicantOrthopedic Systems, Inc.
Decision Date1987-12-30
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CTI STRAIGHT STEM is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1987-12-30 under 510(k) number K873627. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CTI STRAIGHT STEM?

CTI STRAIGHT STEM is a medical device that received FDA 510(k) clearance on 1987-12-30. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K873627.

When did CTI STRAIGHT STEM receive FDA 510(k) clearance?

CTI STRAIGHT STEM received FDA 510(k) clearance on 1987-12-30, under 510(k) number K873627.

Who is the listed applicant for CTI STRAIGHT STEM?

The FDA 510(k) record lists Orthopedic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CTI STRAIGHT STEM?

The FDA product code for CTI STRAIGHT STEM is JDG.

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.

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Other records listing Orthopedic Systems, 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.

K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMK920256SPINE MOTION ANALYZER WITH EMGK910736JACKSON MULTIPURPOSE OPERATING TABLEK910031PARK CITY SHOULDER POSITIONERK903938C FIT CUPK892503NUFFIELD TOTAL KNEE

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Related Devices (Code: JDG)

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.

K212431Biomet Answer/Impact/Integral Distal Centralizer/Centering SleeveBiomet, Inc.K193546Distal CentralizersBiomet, Inc.K173499Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral HeadsStryker OrthopaedicsK001984PROGENY FORGED COCR CEMENTED FEMORAL COMPONENTStelkast CompanyK992234THE TAPER-FIT TOTAL HIP SYSTEMCorin USAK962002AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEMExactech, 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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