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FDA 510(k)

TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER

K-Number: K922308 · 1993-01-12

ApplicantTi-Mesh, Inc.
Decision Date1993-01-12
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER is the device name listed in this FDA 510(k) record. The listed applicant is Ti-Mesh, Inc.. It received FDA 510(k) clearance on 1993-01-12 under 510(k) number K922308. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER?

TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER is a medical device that received FDA 510(k) clearance on 1993-01-12. The listed applicant is Ti-Mesh, Inc.. The 510(k) number is K922308.

When did TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER receive FDA 510(k) clearance?

TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER received FDA 510(k) clearance on 1993-01-12, under 510(k) number K922308.

Who is the listed applicant for TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER?

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

What is the FDA product code for TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER?

The FDA product code for TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER is FTM.

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.

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Other records listing Ti-Mesh, 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.

K923419TISMESH SYSTEMK923802TIMESH TITANIUM MINI-SOFTPLATE/SCREW

Related Devices (Code: FTM)

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.

K262406EluPro Antibiotic-Eluting BioEnvelopeBoston ScientificK250598Endoform Reconstructive Template - PLGAAroa Biosurgery , Ltd.K243595OviTex PRS (Long-Term Resorbable)TELA Bio, Inc.K233991CanGaroo RM Antibacterial EnvelopeElutia, Inc.K241126OviTex PRSTELA Bio, Inc.K223052Peri-Guard and Supple Peri-GuardSynovis Life Technologies, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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