A Preliminary, Non-comparative Study to Evaluate a Bioresorbable Wound Scaffold in Acute Wounds

Inclusion Criteria: * Subjects over 18 years, willing and able to provide written informed consent. * Subjects who have an excised pilonidal sinus wound left to heal by secondary intent. * Subjects who are willing to commit to having two biopsies being taken during the study. Exclusion Criteria: * Subjects with a history of skin sensitivity to any of the components of the study product * Subjects whose wound is infected * Subjects who have participated in a previous clinical study within the past 3 months * Subjects' with a known history of poor compliance with medical treatments * Subjects who are pregnant (where pregnancy is a possibility, a pregnancy testing kit will be provided) * Necrotic/sloughy wounds unless surgically debrided prior to enrolment * Medical or emotional risk associated with the potential biopsy that outweighs the risk of not taking a biopsy as determined by the investigator * Subjects exhibiting any other medical condition which, according to the Investigator, justifies the subject's exclusion from the study * Subjects with impaired renal function