FDA 510(k)

3M PRECISE BRAND INTERNAL SURGICAL STAPLES

K-Number: K921051 · 1992-07-16

Decision Date1992-07-16

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

3M PRECISE BRAND INTERNAL SURGICAL STAPLES is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Ltd.. It received FDA 510(k) clearance on 1992-07-16 under 510(k) number K921051. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M PRECISE BRAND INTERNAL SURGICAL STAPLES?

3M PRECISE BRAND INTERNAL SURGICAL STAPLES is a medical device that received FDA 510(k) clearance on 1992-07-16. The listed applicant is 3M Health Care, Ltd.. The 510(k) number is K921051.

When did 3M PRECISE BRAND INTERNAL SURGICAL STAPLES receive FDA 510(k) clearance?

3M PRECISE BRAND INTERNAL SURGICAL STAPLES received FDA 510(k) clearance on 1992-07-16, under 510(k) number K921051.

Who is the listed applicant for 3M PRECISE BRAND INTERNAL SURGICAL STAPLES?

The FDA 510(k) record lists 3M Health Care, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M PRECISE BRAND INTERNAL SURGICAL STAPLES?

The FDA product code for 3M PRECISE BRAND INTERNAL SURGICAL STAPLES is GDW.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing 3M Health Care, Ltd. as applicant

K953904SARNS 9000 UNIVERSAL ROLLER PUMP K926364ATTEST BRAND RAPID READOUT BIOLOGICAL IND. #129X K941534MODULAR VS-22 CEMENTED FEMORAL HIP SYSTEM K941748STERI-VAC GAS STERILIZER MODEL 8XL K9306813M PREVENTION FABRIC SURGICAL GOWN #78XX K9323073M MAXI-DRIVER II DBATTERY POWERED SYSTEM

View all 49 devices →

Related Devices (Code: GDW)

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.