Identity
- Trade Name
- IJS FDA UDI
- Generic Name
- General internal orthopaedic fixation system implantation kit FDA UDI
- Device Name
- IJS-E Base Plate Assembly FDA UDI
- Model / Reference
- IJS-E Base Plate Assembly FDA UDI
- Description
- IJS-E Base Plate Assembly FDA UDI
Identifiers
- Catalog Number
- IJS-ELB-BPA FDA UDI
- Primary DI / UDI-DI
- 00841506104904 FDA UDI
- 510(k) Number
- K153208 FDA UDI
- FDA Product Code
- LXT FDA UDIOZI FDA UDI
- GMDN Term
- General internal orthopaedic fixation system implantation kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: General internal orthopaedic fixation system implantation kit
Ijs by Skeletal Dynamics L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General internal orthopaedic fixation system implantation kit.
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- ACUMED — ACUMED LLC · Class I
- OsteoMed — Osteomed Corp. · Class II
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Cleared under the same submission
K153208 also covers:
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
- IJS — SKELETAL DYNAMICS L.L.C.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Skeletal Dynamics L.l.c.
Sources (1)
- FDA UDI 0806e16d-8a96-444d-bcbf-f59641e5d3ad 36 fields · synced May 30, 2026