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FDA 510(k)

AXIAL COMPRESSION SCREW

K-Number: K870786 · 1987-06-01

ApplicantStraub Clinic and Hospital
Decision Date1987-06-01
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AXIAL COMPRESSION SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Straub Clinic and Hospital. It received FDA 510(k) clearance on 1987-06-01 under 510(k) number K870786. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIAL COMPRESSION SCREW?

AXIAL COMPRESSION SCREW is a medical device that received FDA 510(k) clearance on 1987-06-01. The listed applicant is Straub Clinic and Hospital. The 510(k) number is K870786.

When did AXIAL COMPRESSION SCREW receive FDA 510(k) clearance?

AXIAL COMPRESSION SCREW received FDA 510(k) clearance on 1987-06-01, under 510(k) number K870786.

Who is the listed applicant for AXIAL COMPRESSION SCREW?

The FDA 510(k) record lists Straub Clinic and Hospital as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AXIAL COMPRESSION SCREW?

The FDA product code for AXIAL COMPRESSION SCREW is KTT.

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 Straub Clinic and Hospital 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.

K883715AXIAL COMPRESSION SCREW

Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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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