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FDA 510(k)

SMILJANIC BONE REPOSITIONING FORCEPS

K-Number: K871535 · 1987-05-14

ApplicantLink America, Inc.
Decision Date1987-05-14
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SMILJANIC BONE REPOSITIONING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Link America, Inc.. It received FDA 510(k) clearance on 1987-05-14 under 510(k) number K871535. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMILJANIC BONE REPOSITIONING FORCEPS?

SMILJANIC BONE REPOSITIONING FORCEPS is a medical device that received FDA 510(k) clearance on 1987-05-14. The listed applicant is Link America, Inc.. The 510(k) number is K871535.

When did SMILJANIC BONE REPOSITIONING FORCEPS receive FDA 510(k) clearance?

SMILJANIC BONE REPOSITIONING FORCEPS received FDA 510(k) clearance on 1987-05-14, under 510(k) number K871535.

Who is the listed applicant for SMILJANIC BONE REPOSITIONING FORCEPS?

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

What is the FDA product code for SMILJANIC BONE REPOSITIONING FORCEPS?

The FDA product code for SMILJANIC BONE REPOSITIONING FORCEPS is HTD.

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Other records listing Link America, 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.

K972760LINK, ACETABULAR REVISION MESH CUPK964458ELLIS EXTERNAL MINI-FIXATOR SYSTEMK955296LINK MP RECONSTRUCTION HIPK954186SLED UNICOMPARTMENT KNEE SYSTEMK931571LINK CERAMIC HEADS 12/14 X 32MMK931572LINK CERAMIC HEADS 14/16 X 32MM

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Related Devices (Code: HTD)

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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, 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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