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FDA 510(k)

ANTERIOR SPINAL FIXATION PLATE

K-Number: K870085 · 1987-06-30

ApplicantTerray Manufacturing, Inc.
Decision Date1987-06-30
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANTERIOR SPINAL FIXATION PLATE 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 1987-06-30 under 510(k) number K870085. 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 ANTERIOR SPINAL FIXATION PLATE?

ANTERIOR SPINAL FIXATION PLATE is a medical device that received FDA 510(k) clearance on 1987-06-30. The listed applicant is Terray Manufacturing, Inc.. The 510(k) number is K870085.

When did ANTERIOR SPINAL FIXATION PLATE receive FDA 510(k) clearance?

ANTERIOR SPINAL FIXATION PLATE received FDA 510(k) clearance on 1987-06-30, under 510(k) number K870085.

Who is the listed applicant for ANTERIOR SPINAL FIXATION PLATE?

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 ANTERIOR SPINAL FIXATION PLATE?

The FDA product code for ANTERIOR SPINAL FIXATION PLATE is KWP.

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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 TRAYK870082BONE PLATE

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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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