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FDA 510(k)

ANVIL RETRACTOR

K-Number: K830585 · 1983-05-27

ApplicantTwin City Surgical, Inc.
Decision Date1983-05-27
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANVIL RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Twin City Surgical, Inc.. It received FDA 510(k) clearance on 1983-05-27 under 510(k) number K830585. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANVIL RETRACTOR?

ANVIL RETRACTOR is a medical device that received FDA 510(k) clearance on 1983-05-27. The listed applicant is Twin City Surgical, Inc.. The 510(k) number is K830585.

When did ANVIL RETRACTOR receive FDA 510(k) clearance?

ANVIL RETRACTOR received FDA 510(k) clearance on 1983-05-27, under 510(k) number K830585.

Who is the listed applicant for ANVIL RETRACTOR?

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

What is the FDA product code for ANVIL RETRACTOR?

The FDA product code for ANVIL RETRACTOR is GAD.

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 Twin City Surgical, 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.

K870767THE (CROM) TESTERK861632SIMS CHAIRK820659A CALIPERK820660A HOOK DRIVERK813067SPINAL WRENCH

Related Devices (Code: GAD)

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.

K152538JRP Wound SpreaderJ.R. Parker, LLCK151104OTELO LLSpineartK132645THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADESMedtronic, Inc.K071775DASHEzsurgicalK050256APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTORApple Medical Corp.K043602QUADRANT RETRACTOR SYSTEMMedtronic Sofamor Danek

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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