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FDA 510(k)

STAINLESS STEEL SUTURE 316L

K-Number: K830522 · 1983-03-31

ApplicantSharpoint, Inc.
Decision Date1983-03-31
Product Code
DecisionSubstantially Equivalent

Device Summary

STAINLESS STEEL SUTURE 316L is the device name listed in this FDA 510(k) record. The listed applicant is Sharpoint, Inc.. It received FDA 510(k) clearance on 1983-03-31 under 510(k) number K830522. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAINLESS STEEL SUTURE 316L?

STAINLESS STEEL SUTURE 316L is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Sharpoint, Inc.. The 510(k) number is K830522.

When did STAINLESS STEEL SUTURE 316L receive FDA 510(k) clearance?

STAINLESS STEEL SUTURE 316L received FDA 510(k) clearance on 1983-03-31, under 510(k) number K830522.

Who is the listed applicant for STAINLESS STEEL SUTURE 316L?

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

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Other records listing Sharpoint, 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.

K863595COATED SUTURE NEEDLEK861947SURGICAL KNIFEK840764EAR KNIVESK840855CORNEAL SCLERAL LANCEK840659ANTERIOR CAPSULECTOMY CYSTITOMEK840660POSTERIOR CAPSULOTOMY CYSTITOME

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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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