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FDA 510(k)

RD 140 SURGICAL BENDER

K-Number: K870084 · 1987-01-28

ApplicantTerray Manufacturing, Inc.
Decision Date1987-01-28
Product CodeHXW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RD 140 SURGICAL BENDER is the device name listed in this FDA 510(k) record. The listed applicant is Terray Manufacturing, Inc.. It received FDA 510(k) clearance on 1987-01-28 under 510(k) number K870084. The device is classified under product code HXW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RD 140 SURGICAL BENDER?

RD 140 SURGICAL BENDER is a medical device that received FDA 510(k) clearance on 1987-01-28. The listed applicant is Terray Manufacturing, Inc.. The 510(k) number is K870084.

When did RD 140 SURGICAL BENDER receive FDA 510(k) clearance?

RD 140 SURGICAL BENDER received FDA 510(k) clearance on 1987-01-28, under 510(k) number K870084.

Who is the listed applicant for RD 140 SURGICAL BENDER?

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

What is the FDA product code for RD 140 SURGICAL BENDER?

The FDA product code for RD 140 SURGICAL BENDER is HXW.

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Other records listing Terray Manufacturing, 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.

K910874THORACIC ANTERIOR SPINAL FIXATION PLATEK882934CASF CANCELLOUS BONE SCREW, BT650K882871CASF DRILL GUIDE DG 170K883193CASF STERILIZATION TRAYK883125CASF STERILIZATION TRAYK870085ANTERIOR SPINAL FIXATION PLATE

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Related Devices (Code: HXW)

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.

K872949ACROMED BONE PLATE BENDERBuckman Co., Inc.K870668DRIVER-BENDER-EXTRACTOR, BONE PINMilitary Engineering, 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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