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FDA 510(k)

MODIFIED PGL ABSORBABLE STAPLE*

K-Number: K900069 · 1990-04-16

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1990-04-16
Product CodeGDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED PGL ABSORBABLE STAPLE* is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K900069. The device is classified under product code GDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED PGL ABSORBABLE STAPLE*?

MODIFIED PGL ABSORBABLE STAPLE* is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K900069.

When did MODIFIED PGL ABSORBABLE STAPLE* receive FDA 510(k) clearance?

MODIFIED PGL ABSORBABLE STAPLE* received FDA 510(k) clearance on 1990-04-16, under 510(k) number K900069.

Who is the listed applicant for MODIFIED PGL ABSORBABLE STAPLE*?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED PGL ABSORBABLE STAPLE*?

The FDA product code for MODIFIED PGL ABSORBABLE STAPLE* is GDG.

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Other records listing United States Surgical, A Division of Tyco Healthc 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.

K071406AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIERK071920AUTOSUTURE ABSORBABLE TACK AND APPLICATORK061288AUTO SUTURE ENDO CLIP III 5 MM CLIP APPLIERK062850AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERSK062326AUTOSUTURE MODIFIED VERSAPORT TROCAR WITH FIXATION SLEEVEK061095AUTO SUTUR ENDO GIA STAPLERS

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Related Devices (Code: GDG)

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.

K891898SKIN HOOKS, VARIOUS TYPESZinnanti Surgical Instruments, Inc.K864425RAYLOR(TM) DISSECTING HOOKCedar Surgical, Inc.K843136BRIMFIELD CANNULATED GRASPING HOOKSBrimfield Scientific InstrumentsK841010SURGICAL HOOKS, VARIOUSPremier Dental Products Co.K812562SURGICAL RETRACTOR & ELASTIC STAYS, DISPHumboldt ProductsK791120MIDDLE EAR PICKS, HOOKS CURETTES,Xomed, 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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