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FDA 510(k)

MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM

K-Number: K854770 · 1986-02-11

ApplicantAdvanced Biosearch Assn.
Decision Date1986-02-11
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Biosearch Assn.. It received FDA 510(k) clearance on 1986-02-11 under 510(k) number K854770. 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 MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM?

MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM is a medical device that received FDA 510(k) clearance on 1986-02-11. The listed applicant is Advanced Biosearch Assn.. The 510(k) number is K854770.

When did MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM receive FDA 510(k) clearance?

MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM received FDA 510(k) clearance on 1986-02-11, under 510(k) number K854770.

Who is the listed applicant for MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM?

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

What is the FDA product code for MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM?

The FDA product code for MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM is KWP.

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Other records listing Advanced Biosearch Assn. 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.

K905514AUTOGENESIS(TM) AUTOMATORK883888CATHSCANNER INTRAVASCULAR ULTRASONIC IMAGING SYST.K855030CHAMPY BONE PLATES & BONE SCREWSK855031MANUAL SURGICAL INSTRUMENTS & ACCESS.CHAMPY BONE PK853916P.M. HIP-FEMORAL PROSTHESISK852839FREEMAN HIP

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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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