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FDA 510(k)

KAMBIN LAMINECTOMY FRAME

K-Number: K874494 · 1987-11-23

ApplicantAvec Scientific Design Corp.
Decision Date1987-11-23
Product CodeLWG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KAMBIN LAMINECTOMY FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Avec Scientific Design Corp.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K874494. The device is classified under product code LWG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAMBIN LAMINECTOMY FRAME?

KAMBIN LAMINECTOMY FRAME is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Avec Scientific Design Corp.. The 510(k) number is K874494.

When did KAMBIN LAMINECTOMY FRAME receive FDA 510(k) clearance?

KAMBIN LAMINECTOMY FRAME received FDA 510(k) clearance on 1987-11-23, under 510(k) number K874494.

Who is the listed applicant for KAMBIN LAMINECTOMY FRAME?

The FDA 510(k) record lists Avec Scientific Design Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KAMBIN LAMINECTOMY FRAME?

The FDA product code for KAMBIN LAMINECTOMY FRAME is LWG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Avec Scientific Design Corp. 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.

K883295CHOP SPINE FRAMEK872544IRRIGATION PRESSURE MONITORK871981BILATERAL CONTINUOUS PASSIVE MOTION DEVICEK871900OVER DRAPE LEG HOLDERK871982TOURNIQUET PRESSURE REGULATOR

Related Devices (Code: LWG)

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.

K883295CHOP SPINE FRAMEAvec Scientific Design Corp.K882520SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADSKarlin Technology, Inc.K873690CEDAR(TM) PELVIC CUSHIONCedar Surgical, 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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