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Composite Cultured Skin

Page Type
Product Code
Definition
For patients with mitten hand deformities due to Recessive Dystrophic Epidermolysis Bullosa (RDEB)
Physical State
Composite Cultured Skin (CCS) is an aseptically processed wound dressing composed of a bovine collagen matrix (coated sponge) in which normal human allogeneic skin cells (epidermal keratinocytes and dermal fibroblasts) are cultured in two layers. The device measures approximately 6 cm x 6 cm (minimally 36 cm2).
Technical Method
Device fucntions as a phsycia l cover of a autograft wound site. It provdies a mosit wound healign environment and physiological components that interact with the acute wound.
Target Area
Wounds created during surgical release of hand contractures (i.e., "mitten" hand deformities).
Regulation Medical Specialty
General and Plastic Surgery
Review Panel
General and Plastic Surgery
Submission Type
HDE - Humanitarian Device Exemption
Device Classification
F
Regulation Number
878.4024
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code PBD is linked to regulation 21CFR878.4024, which does not seem to exist yet. It may be pending at the moment.

Composite Cultured Skin

Page Type
Product Code
Definition
For patients with mitten hand deformities due to Recessive Dystrophic Epidermolysis Bullosa (RDEB)
Physical State
Composite Cultured Skin (CCS) is an aseptically processed wound dressing composed of a bovine collagen matrix (coated sponge) in which normal human allogeneic skin cells (epidermal keratinocytes and dermal fibroblasts) are cultured in two layers. The device measures approximately 6 cm x 6 cm (minimally 36 cm2).
Technical Method
Device fucntions as a phsycia l cover of a autograft wound site. It provdies a mosit wound healign environment and physiological components that interact with the acute wound.
Target Area
Wounds created during surgical release of hand contractures (i.e., "mitten" hand deformities).
Regulation Medical Specialty
General and Plastic Surgery
Review Panel
General and Plastic Surgery
Submission Type
HDE - Humanitarian Device Exemption
Device Classification
F
Regulation Number
878.4024
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code PBD is linked to regulation 21CFR878.4024, which does not seem to exist yet. It may be pending at the moment.