SHERLOCK THREADED SUTURE ANCHOR (TIN COATED)
K-Number: K982169 · 1998-09-14
Device Summary
Frequently Asked Questions
What is the SHERLOCK THREADED SUTURE ANCHOR (TIN COATED)?
SHERLOCK THREADED SUTURE ANCHOR (TIN COATED) is a medical device that received FDA 510(k) clearance on 1998-09-14. The listed applicant is Doctor'S Research Group, Inc.. The 510(k) number is K982169.
When did SHERLOCK THREADED SUTURE ANCHOR (TIN COATED) receive FDA 510(k) clearance?
SHERLOCK THREADED SUTURE ANCHOR (TIN COATED) received FDA 510(k) clearance on 1998-09-14, under 510(k) number K982169.
Who is the listed applicant for SHERLOCK THREADED SUTURE ANCHOR (TIN COATED)?
The FDA 510(k) record lists Doctor'S Research Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHERLOCK THREADED SUTURE ANCHOR (TIN COATED)?
The FDA product code for SHERLOCK THREADED SUTURE ANCHOR (TIN COATED) is MBI.
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.
Other records listing Doctor'S Research Group, 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.
Related Devices (Code: MBI)
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.
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.