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FDA 510(k)

ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER

K-Number: K813170 · 1982-02-12

ApplicantSurgeons Choice, Inc.
Decision Date1982-02-12
Product CodeGAG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER is the device name listed in this FDA 510(k) record. The listed applicant is Surgeons Choice, Inc.. It received FDA 510(k) clearance on 1982-02-12 under 510(k) number K813170. The device is classified under product code GAG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER?

ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER is a medical device that received FDA 510(k) clearance on 1982-02-12. The listed applicant is Surgeons Choice, Inc.. The 510(k) number is K813170.

When did ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER receive FDA 510(k) clearance?

ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER received FDA 510(k) clearance on 1982-02-12, under 510(k) number K813170.

Who is the listed applicant for ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER?

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

What is the FDA product code for ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER?

The FDA product code for ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER is GAG.

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 Surgeons Choice, 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.

K851121PI-PHEUMO INTESTINAL INSTRUMENT SETK851122PI-PNEUMO INTESTINAL STAPLING CARTRIDGEK843399SURGEONS CHOICE PI VASCULAR STAPLINGK830768DISPOSABLE SKIN STAPLERK823776PI-PNEUMO-INTESTINAL INSTRUMENT SET

Related Devices (Code: GAG)

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.

K253527Tri-Staple™ 2.0 Black Circular Reload 21mm Extra Thick (SIGCIR21XT); Tri-Staple™ 2.0 Black Circular Reload 25mm Extra Thick (SIGCIR25XT)Covidien, LLCK251482AEON™ Endoscopic Powered StaplerLexington Medical, Inc.K243596da Vinci SP SureForm 45 Staplers and Reloads (SP1098)Intuitive Surgical, Inc.K240881Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL)Covidien (Part of Medtronic)K241629ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm Standard Stapler (ECH45S); Echelon 3000 45mm Long Stapler (ECH45L); Echelon 3000 60mm Compact Stapler (ECH60C); Echelon 3000 60mm Standard Stapler (ECH60S); Echelon 3000 60mm Long Stapler (ECH60L)Ethicon Endo-Surgery, LLCK234039AEON Endoscopic Powered Stapler (Short/AEPH060); AEON Endoscopic Powered Stapler (Medium/AEPH160); AEON Endoscopic Powered Stapler (Long/AEPH260)Lexington Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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